Traditionally, primary immune deficiencies have been defined based on increased susceptibility to recurrent and/or severe infections. However, immune dysregulation, manifesting with autoimmunity or hyperinflammatory disease, has emerged as a common feature. This is especially true in patients affected by combined immune deficiency (CID), a group of disorders caused by genetic defects that impair, but do not completely abolish, T-cell function. Hypomorphic mutations in the recombination activating genes RAG1 and RAG2 represent the prototype of the broad spectrum of clinical and immunological phenotypes associated with CID. The study of patients with RAG deficiency and with other forms of CID has revealed distinct abnormalities in central and peripheral T- and B-cell tolerance as the key mechanisms involved in immune dysregulation. Understanding the pathophysiology of autoimmunity and hyperinflammation in these disorders may also permit more targeted therapeutic interventions.

Historically, primary immune deficiencies (PIDs) have been defined based on an increased susceptibility to infections. However, it has become increasingly evident that immune dysregulation is an important component of several forms of PID and, in fact, represents the main manifestation in “Diseases of immune dysregulation” listed in the most recent classification of PIDs from the International Union of Immunological Societies (IUIS).1  In addition to these disorders, other forms of PIDs may include autoimmunity or excessive inflammation as part of the clinical phenotype. In a survey of 2183 patients reported to the French PID registry, 571 (26.2%) had ≥1 autoimmune or inflammatory condition, with common variable immune deficiency and combined immune deficiencies (CIDs) being associated with the highest risk of immune dysregulation2 .

According to the IUIS classification, defects resulting in combined defects of cellular and humoral immunity include a heterogeneous group of 49 disorders characterized by a reduced number and/or function of T cells.1  Based on the severity of the T-cell defect, inborn errors of cellular and humoral immunity are further classified into “severe combined immune deficiencies” (SCIDs) and other CIDs, in which the immunological defect is generally less profound.1  The Primary Immune Deficiency Treatment Consortium has developed diagnostic criteria for typical and atypical forms of SCID, with the latter having slightly higher T-cell count and function.3  Diagnostic criteria for CIDs other than SCID have been proposed by the European Society for Immune Deficiencies.4  A different distribution of genotypes has been reported in SCID and CID1,5,6 ; however, mutations in the same gene may associate with a broad spectrum of clinical and immunological phenotypes, as best exemplified by defects in the recombinase activating genes RAG1 and RAG2.7  Immune dysregulation is more commonly observed in patients with CID than in those with SCID2 ; in the latter, it is more frequent among patients with atypical SCID (AS),8  indicating that subnormal (but not absent) T-cell mediated immunity is a permissive factor. Manifestations of immune dysregulation in CID may include systemic and organ-specific autoimmunity and inflammatory complications; however, autoimmune cytopenias are more frequently observed.2,6,7  Importantly, immune dysregulation represents a negative prognostic factor for survival in patients with CID, even for patients who are eventually treated by hematopoietic stem cell transplantation (HSCT).2  Altogether, these data indicate the importance of prompt recognition and treatment of immune dysregulation in patients with CID. Finally, the study of these patients is illustrative of how different degrees of impairment of T- and B-cell development and function translates in defective adaptive immune responses against nonself antigens, as well as perturbs immune homeostasis by affecting central and peripheral mechanisms of immune tolerance.9  Here, we will review the clinical manifestations, the laboratory findings, and the pathophysiology of immune dysregulation associated with RAG deficiency and other forms of CID (Table 1).

The recombination activating proteins (RAG1 and RAG2) initiate the process of V(D)J recombination, allowing for the formation of a diverse repertoire of T-cell receptors (TCRs) in T cells and immunoglobulins (Igs) in B cells.10  This process is essential for the generation of polyclonal T and B cells with a broad antigen-recognition capacity.11,12  Biallelic RAG mutations were initially associated with SCID with absent T and B cells (TBSCID).13  Subsequently, the clinical presentation of RAG deficiency expanded to include Omenn syndrome (OS), in which residual RAG protein activity allows for the generation of oligoclonal T cells.14,15 

Patients with OS present in infancy with life-threatening infections, erythroderma, lymphadenopathy, hepatosplenomegaly, eosinophilia, and severe hypogammaglobulinemia with increased IgE levels. They typically have absent B cells and expanded activated populations of autologous autoreactive T cells that infiltrate the skin, gut, liver, and other organs. Interestingly, within the same patient with OS, the T cells that infiltrate distinct organs carry distinct TCR specificities, suggesting tissue-specific self-antigen–driven expansion of T-cell clonotypes.16 

Hypomorphic RAG mutations may also cause AS,17  in which patients have variable, but reduced, numbers of T and B cells with a decreased proportion of naive T cells. Patients with AS are highly susceptible to severe and opportunistic infections8 ; however, in contrast to typical SCID, they are at high risk for autoimmune manifestations, especially cytopenias.7,8  A distinct form of AS associated with oligoclonal expansion of TCRγδ+ T cells and an increased risk for autoimmune hemolytic anemia upon cytomegalovirus (CMV) infection has been reported in RAG deficiency.18,19 

More recently, RAG mutations have also been detected in patients with delayed-onset disease exhibiting granulomas and/or autoimmune manifestations (CID-G/AI phenotype).7,8,20-25  In these patients, T and B cells are usually present, in vitro T-cell proliferation to mitogens is often normal or slightly reduced, and IgG levels and antibody responses to immunization may be variably preserved. In this group of patients, early-onset severe infections are infrequent, but late-onset immune dysregulation and infections cause significant morbidity.7,8  In particular, recurrent respiratory tract infections leading to bronchiectasis and chronic and recurrent viral infections due to herpesviruses and human papillomavirus are common in CID-G/AI.7,8 

Overall, these observations show that immune dysregulation is a prominent manifestation of impaired RAG function that is especially common among patients exhibiting SCID or CID-G/AI.

In a cohort of 424 patients with RAG deficiency, autoimmunity and/or granulomatous lesions occurred in 6.5% of patients with OS, 45% of patients with AS, and 89% of patients with CID-G/AI and other delayed-onset phenotypes.7  Cytopenias were the leading autoimmune manifestation, with 55% (74/134) of AS and CID-G/AI patients presenting with autoimmune hemolytic anemia, immune thrombocytopenic purpura, or autoimmune neutropenia and 26% suffering from ≥2 autoimmune cytopenias. Other autoimmune phenomena occurred in skin, vasculature, gut, endocrine organs, and neuronal and kidney tissues. Along with these manifestations of autoimmunity, a broad range of autoantibodies, including neutralizing antibodies to interleukin-12 (IL-12), interferon-α (IFN-α), and IFN-ω, were detected in patients with CID-G/AI.26  Severe varicella was reported in some of these patients, suggesting that the presence of these anti-cytokine antibodies may increase the risk of infections or that, alternatively, varicella may trigger autoimmunity.

Granulomas, found in 35% of the patients with CID-G/AI, were predominantly localized in the skin, but were also observed in lungs, liver, soft tissues, spleen, gut, testis, bone marrow, and pancreas.7 

In another series of 63 patients with RAG deficiency with prominent autoimmune and/or hyperinflammatory manifestations (most of whom belonged to the AS and CID-G/AI phenotypes), 84.1% had autoimmune cytopenias, 23.8% had granulomas, and 19% had skin manifestations.8  In this cohort, autoimmune cytopenias were often the presenting sign of disease and were frequently refractory to treatment with IV Ig, steroids, and rituximab. Similarly, granulomas, vasculitis, and enteropathy often failed to respond to first- and second-line immunosuppressive treatment, including steroids, IV Ig, cyclophosphamide, infliximab, cyclosporine, and sirolimus. Treatment-refractory autoimmunity and/or hyperinflammation were an indication of HSCT in 20 patients.

Various mechanisms contribute to the complexity and severity of immune dysregulation in patients with hypomorphic RAG mutations. In the normal thymus, developing T cells expressing self-reactive specificities are subjected to negative selection upon high-affinity interaction with thymic epithelial cells (TECs) and thymic dendritic cells presenting self-antigens in the context of major histocompatibility molecules. The first such wave of negative selection occurs in the cortex; depletion of T-cell clonotypes containing cysteine residues at the center of the TCR-CDR3 has recently been identified as a biomarker of this first wave of negative selection.27  A second wave of negative selection occurs in the thymic medulla, when autoreactive T cells binding with high-affinity self-peptides are deleted or, alternatively, are diverted to become regulatory T cells (Tregs). Importantly, developing T cells provide instructional signals to medullary TECs (mTECs), allowing their maturation and promoting expression of autoimmune regulator, a transcriptional activator that induces expression of tissue-restricted antigens by mTECs.28  A biomarker of this second wave of negative selection is represented by purging of TCR clonotypes containing hydrophobic amino acids at positions 6 and 7 of the TCR-CDR3.29  In contrast to what is observed in healthy individuals, the thymus of RAG-deficient patients has an abnormal architecture.23,30  Defective cross talk between TECs and the few thymocytes that are able to overcome the differentiation block results in impairment of negative selection. The high frequency of peripheral TCR clonotypes containing central cysteine27  is indicative of impairment of wave 1 deletion of self-reactive thymocytes in the thymus cortex. In the medulla, defective thymopoiesis causes impaired maturation of mTECs, as well as reduced expression of autoimmune regulator and tissue-restricted antigens.31  Peripheral T cells from RAG-mutated patients express TCR clonotypes with an increased frequency of hydrophobic amino acids at positions 6 and 7 of the CDR3, indicating impairment of the second wave of negative selection, as well.27,32  Tregs are present in low number, display a restricted repertoire,32,33  and have reduced suppressive function.33-35 

Finally, the few oligoclonal T cells that egress the thymus undergo homeostatic proliferation in the periphery. In this setting, increased cytokine production may also contribute to inflammation and autoimmunity. Abnormalities of rearrangements at the TCRα locus may also contribute to immune dysregulation in patients with hypomorphic RAG mutations. During normal thymocyte development, multiple waves of V(D)J recombination are required for the expression of distal TRAV genes. Patients with hypomorphic RAG mutations show a dramatic reduction in T cells expressing the products of distal TRAV genes, including TRAV1-2.36  The TRAV1-2 product (Vα7.2) is part of the semi-invariant TCR expressed by human mucosa-associated invariant T cells, which serve an important homeostatic function at mucosal surfaces by recognizing microbial-derived vitamin B metabolism products.37  The reduced number of mucosa-associated invariant T cells may contribute to immune dysregulation at the mucosal surface level and dysbiosis in RAG deficiency.38  Finally, defective V(D)J recombination activity also affects the development of invariant natural killer T cells, another important immunoregulatory subset.34,39  Altogether, abnormalities in T-cell repertoire diversity and composition have important implications for immune deficiency and the immune dysregulation of RAG deficiency. A reduced diversity translates into an impaired capacity to recognize nonself antigens, causing increased susceptibility to infections. On the other hand, qualitative abnormalities in the composition of the T-cell repertoire, with an increased frequency of clonotypes harboring molecular signatures of self-reactivity, represent a risk factor for autoimmune complications.

RAG deficiency also has important consequences for B-cell development and homeostasis. Despite a block at the pre-B cell stage in the bone marrow and a severe reduction in the number of circulating B cells,40  enzyme-linked immunospot analysis showed that Ig-secreting cells are present in the bone marrow of OS patients,41  and autoantibodies are frequently detected, especially in patients with AS and CID-G/ASI, indicating defects in B-cell tolerance checkpoints.26,42  Reexpression of the RAG genes in the bone marrow at a stage between early immature and immature B cells reduces the proportion of autoreactive B cells (a process known as “receptor editing”).43  Impaired receptor editing has been demonstrated in patients and mice with hypomorphic RAG mutations.15,40,41  In the periphery, a second B-cell tolerance checkpoint takes place at the transition between transitional B cells and mature naive B cells. These 2 populations differ in their levels of expression of B-cell activating factor receptor, which serves as a survival signal. Patients and mouse models with hypomorphic RAG mutations are B-cell lymphopenic, a condition that favors the increased B-cell activating factor levels produced by myeloid cells, promoting survival of transitional B cells and enriching the peripheral B pool in self-reactive B cells.15,35  An increased usage of IGHV4-34, IGHV3-9, IGH4-31, and IGHV3-23 genes, which has been associated with autoreactive B cells,44,45  has been reported in RAG-mutated patients.40,46 

Patients with OS often present with cutaneous and gastrointestinal (GI) clinical manifestations. The possible mechanisms accounting for immune dysregulation in these compartments have been extensively studied in Rag2R229Q mice, a model of OS. Rag2R229Q mice develop spontaneous signs of intestinal disease, with activated T cells infiltrating the gut lamina propria and expressing high levels of CCR9 (a gut-homing receptor) and T helper 1 (Th1) and Th17 cytokines.38  Lack of secretory IgA, which plays a protective role and acts as a bacterial flora modulator, permits intestinal colonization. Along with mucosal inflammation, increased permeability leads to disruption of the gut mucosa barrier and to bacterial translocation, also documented by increased serum levels of lipopolysaccharide.38  Analysis of the microbiota of Rag2R229Q mice showed a reduction in richness and diversity and enrichment of the Proteobacteria phylum, which is also observed in chronic inflammatory conditions.47  Transfer of fecal samples from wild-type mice into Rag2R229Q mice was associated with decreased inflammation and reduction of cellular infiltrates. In contrast, wild-type mice colonized with Rag2R229Q feces developed increased frequencies of inflammatory cells enriched in Th1/Th17 cells in the gut lamina propria and in the spleen.38  Depletion of microflora using antibiotics (metronidazole, vancomycin, ampicillin) had a dramatic impact on gut inflammation,38  further supporting the notion that dysbiosis plays a causative role in immune dysregulation.48 

Finally, a significant proportion of patients with CID-G/AI exhibit extensive granulomas in skin and internal organs.7,8,20,23  The granulomas are characteristically composed of organized inflammatory infiltrates, including centrally localized macrophages and giant cells, a ring of lymphocytes, and variable number of fibroblasts.49  The pathophysiology of granuloma formation remains enigmatic and has not been recapitulated in mouse models carrying mutations equivalent to those identified in patients with CID-G/AI.35  Interestingly, the rubella virus vaccine strain has been detected in granulomatous lesions and other tissue samples of patients with hypomorphic RAG mutations50,51  or with other T-cell defects,52,53  where it establishes chronic infection in M2 macrophages and keratinocytes. It is unknown why only the rubella virus vaccine strain (and not the measles or mumps viruses, for instance) has been identified in the granulomas. Moreover, the observation that granulomas occur at a variable time (often, years) after administration of the rubella vaccine suggests that the immunodeficiency of RAG deficiency plays a critical role in persistence of the attenuated virus, yet additional factors must account for the delayed immunopathology. Mutations of the virus genome and changes in the immune profile of patients (with increased cytokine production associated with ongoing homeostatic proliferation) may play a role in the development of granulomatous lesions.

In addition to RAG deficiency, immune dysregulation is common in patients with other forms of CID. Thymocyte positive and negative selection, as well as generation of thymic Tregs, are largely controlled by the strength of TCR signaling.54  In particular, weak interaction of the TCR with self-peptide–major histocompatibility complex (MHC) prevents death by neglect and promotes thymocyte survival; in contrast, strong agonist-induced TCR signaling causes negative selection of self-reactive thymocytes55  or induction of CD25+ Treg progenitors.56  Genetically determined defects of TCR signaling are associated with altered T-cell tolerance. For example, autoimmune cytopenias, hypothyroidism, and enteropathy have been reported in patients with CD3γ deficiency,57-59  and the study of their T-cell repertoire has revealed molecular signatures of self-reactivity, with a high proportion of clonotypes containing hydrophobic amino acids, along with a reduced number and restricted repertoire of Tregs.59  Hypomorphic ZAP70 mutations have been associated with wheezing, erythroderma, and inflammatory bowel disease,60,61  and a combination of hypomorphic and activating mutations in the same gene has been reported in 2 siblings with severe bullous pemphigoid, colitis, nephrotic syndrome, and autoantibody-induced hemophilia.62  Autoimmune cytopenias and lymphoproliferative disease were prominent signs of immune dysregulation in 3 siblings with LAT deficiency,63  whereas nodular skin lesions with inflammatory infiltrates, autoimmune thrombocytopenia, and retinal vasculitis have been reported in a patient with LCK deficiency.64 

Other forms of CID are due to signaling defects that are not restricted to T cells. The CARD11-BCL10-MALT1 signalosome complex provides a link between triggering of cell surface receptors (including the TCR and the B-cell receptor) to NF-κB signaling.65  Following TCR and B-cell receptor activation, CARD11 is recruited to the immunological synapse, where it is phosphorylated by protein kinase C θ (PKCθ) and PKCβ in T and B cells, respectively.66,67  This allows recruitment of BCL10 and MALT1,68  ultimately leading to NF-κB activation.65  In addition, CARD11 and MALT1 regulate TCR-mediated glutamine uptake and activation of the mTOR pathway.69  Null-CARD11 mutations cause susceptibility to severe infections since early in life, which is associated with an increased proportion of transitional B cells, hypogammaglobulinemia, a predominantly naive T-cell phenotype, severely diminished Treg number, and decreased in vitro T-cell proliferative responses.70  Interestingly, somatic second site reversion allowing partial restoration of CARD11 protein expression and function was associated with an OS-like phenotype, including erythroderma with oligoclonal expansion of skin-infiltrating T cells, hepatosplenomegaly, eosinophilia, and elevated serum IgE.71  In contrast, heterozygous dominant–negative CARD11 mutations are associated with immune dysregulation manifesting as severe atopic disease, associated with Th2 skewing70,72 ; most of these patients also have a history of recurrent respiratory and cutaneous infections, and some also exhibit autoimmunity (colitis, necrotizing granulomas, alopecia).73  In addition to impairing NF-κB activation, these mutations often prevent optimal glutamine uptake in response to TCR stimulation, thereby reducing mTORC1 signaling. MALT1 deficiency is another cause of CID; in addition to infections, these patients also exhibit eczema and inflammatory GI disease, and prominent T-cell infiltrates are often found in skin and GI biopsies.74-76  Interestingly, multiorgan inflammatory disease is also present in Malt1PD/PD mutant mice and is associated with expansion of Th1, Th2, and Th17 cells, high levels of inflammatory cytokines, decreased numbers of IL-10–producing B cells, and a severe defect in Treg number.77 

CD40 ligand (CD40L) is a cell surface molecule that is predominantly expressed by activated CD4+ T cells; upon interaction with its cognate receptor CD40, which is constitutively expressed by B cells and antigen-presenting cells, it plays an important role in regulating B-cell responses and promoting T-cell priming.78  In addition, soluble CD40L released by T cells and platelets plays an important role in modulating inflammatory responses.79  CD40L deficiency is an X-linked CID; it is primarily characterized by susceptibility to severe infections that are often caused by opportunistic pathogens, including Pneumocystis jirovecii, Cryptosporidium spp., Cryptococcus, CMV, and Mycobacteria.80  T-cell responses to Cryptosporidium and CMV infection of the liver and bile ducts play an important role in the development of sclerosing cholangitis.81,82  Moreover, ∼7% to 10% of the patients exhibit immune dysregulation, with thrombocytopenia, hemolytic anemia, seronegative arthritis, hypothyroidism, cutaneous granulomas, and inflammatory bowel disease.83-87  These autoimmune complications may reflect, at least in part, skewing of the IgM repertoire toward self-antigens.88  A severe decrease in circulating T follicular cells, Tregs, and follicular regulatory T cells has been reported in 1 patient with autosomal-recessive CD40 deficiency and in adults with CD40L deficiency,89  supporting the concept that the T-cell abnormalities are a major driver of autoimmunity in this disease. Although autoimmune manifestations are also common in B-cell autonomous forms of hyper-IgM syndromes, such as activation-induced cytidine deaminase deficiency,90  the mechanisms are different. In the absence of functional activation-induced cytidine deaminase, central B-cell tolerance and peripheral B-cell tolerance are affected.91,92  The impairment of somatic hypermutation defect causes persistence of autoreactive B-cell clones prevents production of mutated antibodies that can clear antigens. In this setting, immune activation results in sustained production of cytokines that may negatively affect Treg function.91,92 

MHC class I and class II molecules play a critical role in adaptive immune responses. By allowing peptide binding and presentation to developing thymocytes, they participate in the mechanisms of positive and negative selection, whereas in the periphery they regulate CD8+ and CD4+ responses. Deficiencies in MHC class I and class II molecules are a cause of CID.1  In addition to suffering from recurrent sinopulmonary infections, patients with MHC class I deficiency have a high propensity to develop sterile necrotizing granulomas that predominantly affect the skin but may also involve the lungs and other tissues.93,94  In 1 case, persistence of the vaccine strain of the rubella virus was demonstrated in the skin lesions.53  Autoreactive natural killer cells and TCRγδ+ T cells have been demonstrated in the circulation and in the skin lesions of these patients,94  suggesting that they may play a role in disease pathophysiology. Use of immunosuppressive medications and injection of IFN-α are not helpful and may worsen the lesions.95  Patients with MHC class II deficiency are highly vulnerable to bacterial, viral, and fungal infections and have a high mortality. Autoimmune manifestations, and cytopenias in particular, are seen in ∼20% of patients.93  Defective MHC class II expression on TECs may cause impaired negative selection of self-reactive CD4+ T cells and contribute to skewing of the CD4+ T-cell repertoire.96,97 

Serine threonine kinase 4 (STK4) is a broadly expressed protein upstream of MAPK that controls cell survival and apoptosis. STK4 deficiency in humans is a cause of CID; in addition to increased susceptibility to infections (mostly of viral origin), these patients often exhibit dysgammaglobulinemia with autoantibodies, lymphoproliferative disease, and autoimmune cytopenias, as well as an increased risk for B- and T-cell lymphomas.98-101  It has recently been shown that the mechanisms underlying immune dysregulation in this condition are B-cell autonomous.102  Patients have an increased proportion of transitional B cells and a reduced number of memory B cells, and STK4-deficient mice have a low number of splenic T follicular helper (Tfh) cells, follicular helper B cells, and peritoneal B1a cells, as well as an absence of marginal zone B cells. In response to immunization, Stk4 mutant mice display impaired generation of germinal centers and produce a low number of memory B cells.102  Moreover, although memory B cells from STK4-mutated patients and mice can differentiate into plasma cells, these have an impaired capacity to produce antibodies.102  It is unclear how these B-cell abnormalities are linked to autoimmunity in these patients. One hypothesis is that STK4 deficiency may lead to impaired FOXO1 phosphorylation and nuclear translocation and, consequently, affect germinal center formation and antibody production.102 

IL-21 regulates Tfh cell and regulatory B-cell development and promotes plasma blast generation.103,104  IL-21 deficiency is a form of CID described in a patient who presented with very early-onset inflammatory bowel disease and went on to develop recurrent and severe respiratory tract infections.105  The immunological phenotype included hypogammaglobulinemia, a low number of class-switched memory B cells, a normal number of T cells (but with an increased proportion of TCRγδ+ T cells), and reduced T-cell proliferation in vitro to tetanus toxoid. An inflammatory bowel disease–like picture has been also reported in patients with IL-21R deficiency, although in these cases the GI tract pathology may have been driven by Cryptosporidium infection.106,107  Studies in mice have shown that IL-21/IL-21R signaling protects against dextran sulfate sodium–induced colitis through suppression of Th1 responses and activation of Th2 cell, Th17 cell, and Treg responses.108 

Inducible T-cell costimulator (ICOS) is a costimulatory molecule that regulates T-cell proliferation and cytokine secretion, migration of Tfh cells into the follicles, and production of IL-10 and IL-21, thereby favoring generation of long-lived memory B cells and plasma cells.109,110  In addition, it has recently been shown that ICOS-mediated costimulation imprints the functional stability of FOXP3 required for optimal Treg function in the periphery.111  Human ICOS deficiency was initially identified as a monogenic form of adult-onset common variable immunodeficiency,112  but it has subsequently been included among the causes of CID.1  The disease is characterized by increased susceptibility to bacterial, viral, and opportunistic infections, immune dysregulation, and cancer.113  The immunological phenotype includes hypogammaglobulinemia, impaired specific antibody responses, a reduced number of class-switched memory B cells and circulating Tfh cells, and defective in vitro production of various cytokines.113  In a series of 15 patients, immune dysregulation was documented in 73% of them, and it presented more commonly as enteropathy; however, splenomegaly, psoriasis, arthritis, cytopenias, eczema, granulomas, and interstitial lymphocytic pneumonitis have been also documented that require the use of steroids or other immunosuppressive agents.113  The precise mechanisms underlying immune dysregulation in this disease are not known. A normal number of Tregs has been reported in most patients,113  but reduced expression of CTLA4 has been observed in some cases.114  Finally, the observation that plasmacytoid dendritic cells promote IL-10 production by Tregs via the ICOS ligand115  suggests that a possible defect of this pathway may also contribute to altered peripheral immune tolerance.

Activated phosphoinositide 3-kinase δ syndrome 1 (APDS1) and APDS2 are due to heterozygous mutations in the PIK3CD or PIK3R1 gene; these encode for the p110δ catalytic and the p85α regulatory subunits of the PI3Kδ enzyme, respectively. The mutations cause increased activity of the PI3K-AKT-mTOR pathway. The clinical phenotypes of APDS1 and APDS2 overlap significantly.116  Although both diseases are listed as “Predominantly antibody deficiencies” in the IUIS classification,1  they are indeed CIDs, with increased susceptibility to sinopulmonary infections, recurrent or persistent infections due to Herpesviridae (Epstein-Barr virus, CMV, varicella zoster virus, herpes simplex virus), lymphoproliferation (lymphadenopathy, splenomegaly and nodular lymphoid hyperplasia in the gut and the respiratory tract), autoimmunity (cytopenias, thyroiditis, glomerulonephritis, type 1 diabetes, autoimmune hepatitis, and others), and a high risk for lymphoma.116  The immunological phenotype of APDS includes (1) T-cell abnormalities with decreased naive T cells, increased T effector memory cells and Tfh cells, and accumulation of senescent T cells, and (2) B-cell impairment, as indicated by variable degrees of hypogammaglobulinemia, elevated IgM levels, increased number of transitional B cells, decreased switched memory cells, and impaired response to immunization.117  Functional testing on T and B cells in APDS patients demonstrated increased AKT and S6 phosphorylation due to increased mTOR signaling, thereby supporting the use of mTOR inhibitors to control the disease.118  HSCT has been successful in reversing the clinical phenotype; however, graft failure and viral reactivation posttransplant have been observed.119,120  Characterization of the molecular mechanisms underpinning APDS prompted the use of selective PI3Kδ inhibitors as a possible therapeutic option. An open-label trial with dose-escalating administration of leniolisib for 12 weeks resulted in significant improvement of lymphoproliferation and cytopenias by the end of the treatment.121 

Autoimmunity and lymphoproliferation are increasingly recognized as a primary risk factor for morbidity and mortality in patients with CID. Various mechanisms may contribute to the immune dysregulation that is often observed in patients with CID. The inability to clear infections may result in continuous stimulation of the immune system, increased production of inflammatory cytokines, and tissue damage, as indicated by sclerosing cholangitis following Cryptosporidium or CMV infection in patients with CD40L and CD40 deficiency, as well as by detection of the vaccine rubella virus in granulomas of patients with various forms of CID. However, perturbations in central and peripheral tolerance in T- and/or B-cell compartments also play a major role in causing autoimmunity, hyperinflammatory responses, and increased risk for lymphoproliferation in patients with CID. Improved knowledge of the genetic and molecular mechanisms underpinning immune dysregulation in CID has the potential to provide targeted therapeutic approaches aimed to prevent disease evolution and improve outcome.

This work was supported by the Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health.

Contribution: L.D.N., O.M.D., and A.V. researched data and wrote and reviewed the manuscript.

Conflict-of-interest disclosure: The authors declare no competing financial interests.

Correspondence: Luigi D. Notarangelo, Immune Deficiency Genetics Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Building 10, Room 5-3950, 10 Center Dr, Bethesda, MD 20892; e-mail: luigi.notarangelo2@nih.gov.

1.
Picard
C
,
Bobby Gaspar
H
,
Al-Herz
W
, et al
.
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee report on inborn errors of immunity
.
J Clin Immunol
.
2018
;
38
(
1
):
96
-
128
.
2.
Fischer
A
,
Provot
J
,
Jais
JP
,
Alcais
A
,
Mahlaoui
N
;
members of the CEREDIH French PID study group
.
Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies
.
J Allergy Clin Immunol
.
2017
;
140
(
5
):
1388
-
1393.e8
.
3.
Shearer
WT
,
Dunn
E
,
Notarangelo
LD
, et al
.
Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience
.
J Allergy Clin Immunol
.
2014
;
133
(
4
):
1092
-
1098
.
4.
Seidel
MG
,
Kindle
G
,
Gathmann
B
, et al;
ESID Registry Working Party and collaborators
.
The European Society for Immunodeficiencies (ESID) Registry working definitions for the clinical diagnosis of inborn errors of immunity
.
J Allergy Clin Immunol Pract
.
2019
;
7
(
6
):
1763
-
1770
.
5.
Dvorak
CC
,
Haddad
E
,
Buckley
RH
, et al
.
The genetic landscape of severe combined immunodeficiency in the United States and Canada in the current era (2010-2018)
.
J Allergy Clin Immunol
.
2019
;
143
(
1
):
405
-
407
.
6.
Speckmann
C
,
Doerken
S
,
Aiuti
A
, et al;
P-CID study of the Inborn Errors Working Party of the EBMT
.
A prospective study on the natural history of patients with profound combined immunodeficiency: an interim analysis
.
J Allergy Clin Immunol
.
2017
;
139
(
4
):
1302
-
1310.e4
.
7.
Delmonte
OM
,
Schuetz
C
,
Notarangelo
LD
.
RAG deficiency: two genes, many diseases
.
J Clin Immunol
.
2018
;
38
(
6
):
646
-
655
.
8.
Farmer
JR
,
Foldvari
Z
,
Ujhazi
B
, et al
.
Outcomes and treatment strategies for autoimmunity and hyperinflammation in patients with RAG deficiency
.
J Allergy Clin Immunol Pract
.
2019
;
7
(
6
):
1970
-
1985.e4
.
9.
Liston
A
,
Enders
A
,
Siggs
OM
.
Unravelling the association of partial T-cell immunodeficiency and immune dysregulation
.
Nat Rev Immunol
.
2008
;
8
(
7
):
545
-
558
.
10.
Oettinger
MA
,
Schatz
DG
,
Gorka
C
,
Baltimore
D
.
RAG-1 and RAG-2, adjacent genes that synergistically activate V(D)J recombination
.
Science
.
1990
;
248
(
4962
):
1517
-
1523
.
11.
Notarangelo
LD
,
Kim
MS
,
Walter
JE
,
Lee
YN
.
Human RAG mutations: biochemistry and clinical implications
.
Nat Rev Immunol
.
2016
;
16
(
4
):
234
-
246
.
12.
Fugmann
SD
,
Lee
AI
,
Shockett
PE
,
Villey
IJ
,
Schatz
DG
.
The RAG proteins and V(D)J recombination: complexes, ends, and transposition
.
Annu Rev Immunol
.
2000
;
18
(
1
):
495
-
527
.
13.
Schwarz
K
,
Gauss
GH
,
Ludwig
L
, et al
.
RAG mutations in human B cell-negative SCID
.
Science
.
1996
;
274
(
5284
):
97
-
99
.
14.
Villa
A
,
Santagata
S
,
Bozzi
F
, et al
.
Partial V(D)J recombination activity leads to Omenn syndrome
.
Cell
.
1998
;
93
(
5
):
885
-
896
.
15.
Walter
JE
,
Rucci
F
,
Patrizi
L
, et al
.
Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency
.
J Exp Med
.
2010
;
207
(
7
):
1541
-
1554
.
16.
Signorini
S
,
Imberti
L
,
Pirovano
S
, et al
.
Intrathymic restriction and peripheral expansion of the T-cell repertoire in Omenn syndrome
.
Blood
.
1999
;
94
(
10
):
3468
-
3478
.
17.
Villa
A
,
Sobacchi
C
,
Notarangelo
LD
, et al
.
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations
.
Blood
.
2001
;
97
(
1
):
81
-
88
.
18.
de Villartay
JP
,
Lim
A
,
Al-Mousa
H
, et al
.
A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection
.
J Clin Invest
.
2005
;
115
(
11
):
3291
-
3299
.
19.
Ehl
S
,
Schwarz
K
,
Enders
A
, et al
.
A variant of SCID with specific immune responses and predominance of gamma delta T cells
.
J Clin Invest
.
2005
;
115
(
11
):
3140
-
3148
.
20.
Schuetz
C
,
Huck
K
,
Gudowius
S
, et al
.
An immunodeficiency disease with RAG mutations and granulomas
.
N Engl J Med
.
2008
;
358
(
19
):
2030
-
2038
.
21.
Sharapova
SO
,
Migas
A
,
Guryanova
I
, et al
.
Late-onset combined immune deficiency associated to skin granuloma due to heterozygous compound mutations in RAG1 gene in a 14 years old male
.
Hum Immunol
.
2013
;
74
(
1
):
18
-
22
.
22.
Henderson
LA
,
Frugoni
F
,
Hopkins
G
, et al
.
Expanding the spectrum of recombination-activating gene 1 deficiency: a family with early-onset autoimmunity
.
J Allergy Clin Immunol
.
2013
;
132
(
4
):
969
-
971-972
.
23.
De Ravin
SS
,
Cowen
EW
,
Zarember
KA
, et al
.
Hypomorphic Rag mutations can cause destructive midline granulomatous disease
.
Blood
.
2010
;
116
(
8
):
1263
-
1271
.
24.
Avila
EM
,
Uzel
G
,
Hsu
A
, et al
.
Highly variable clinical phenotypes of hypomorphic RAG1 mutations
.
Pediatrics
.
2010
;
126
(
5
):
e1248
-
e1252
.
25.
Reiff
A
,
Bassuk
AG
,
Church
JA
,
Campbell
E
,
Bing
X
,
Ferguson
PJ
.
Exome sequencing reveals RAG1 mutations in a child with autoimmunity and sterile chronic multifocal osteomyelitis evolving into disseminated granulomatous disease
.
J Clin Immunol
.
2013
;
33
(
8
):
1289
-
1292
.
26.
Walter
JE
,
Rosen
LB
,
Csomos
K
, et al
.
Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency
.
J Clin Invest
.
2016
;
126
(
11
):
4389
.
27.
Daley
SR
,
Koay
HF
,
Dobbs
K
, et al
.
Cysteine and hydrophobic residues in CDR3 serve as distinct T-cell self-reactivity indices
.
J Allergy Clin Immunol
.
2019
;
144
(
1
):
333
-
336
.
28.
Anderson
MS
,
Venanzi
ES
,
Klein
L
, et al
.
Projection of an immunological self shadow within the thymus by the aire protein
.
Science
.
2002
;
298
(
5597
):
1395
-
1401
.
29.
Stadinski
BD
,
Shekhar
K
,
Gómez-Touriño
I
, et al
.
Hydrophobic CDR3 residues promote the development of self-reactive T cells
.
Nat Immunol
.
2016
;
17
(
8
):
946
-
955
.
30.
Poliani
PL
,
Facchetti
F
,
Ravanini
M
, et al
.
Early defects in human T-cell development severely affect distribution and maturation of thymic stromal cells: possible implications for the pathophysiology of Omenn syndrome
.
Blood
.
2009
;
114
(
1
):
105
-
108
.
31.
Cavadini
P
,
Vermi
W
,
Facchetti
F
, et al
.
AIRE deficiency in thymus of 2 patients with Omenn syndrome
.
J Clin Invest
.
2005
;
115
(
3
):
728
-
732
.
32.
Rowe
JH
,
Stadinski
BD
,
Henderson
LA
, et al
.
Abnormalities of T-cell receptor repertoire in CD4+ regulatory and conventional T cells in patients with RAG mutations: implications for autoimmunity
.
J Allergy Clin Immunol
.
2017
;
140
(
6
):
1739
-
1743.e7
.
33.
Cassani
B
,
Poliani
PL
,
Moratto
D
, et al
.
Defect of regulatory T cells in patients with Omenn syndrome
.
J Allergy Clin Immunol
.
2010
;
125
(
1
):
209
-
216
.
34.
Marrella
V
,
Poliani
PL
,
Casati
A
, et al
.
A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndrome
.
J Clin Invest
.
2007
;
117
(
5
):
1260
-
1269
.
35.
Ott de Bruin
LM
,
Bosticardo
M
,
Barbieri
A
, et al
.
Hypomorphic Rag1 mutations alter the preimmune repertoire at early stages of lymphoid development
.
Blood
.
2018
;
132
(
3
):
281
-
292
.
36.
Berland
A
,
Rosain
J
,
Kaltenbach
S
, et al
.
PROMIDISα: a T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects
.
J Allergy Clin Immunol
.
2019
;
143
(
1
):
325
-
334.e2
.
37.
Chandra
S
,
Kronenberg
M
.
Activation and function of iNKT and MAIT cells
.
Adv Immunol
.
2015
;
127
:
145
-
201
.
38.
Rigoni
R
,
Fontana
E
,
Guglielmetti
S
, et al
.
Intestinal microbiota sustains inflammation and autoimmunity induced by hypomorphic RAG defects
.
J Exp Med
.
2016
;
213
(
3
):
355
-
375
.
39.
Matangkasombut
P
,
Pichavant
M
,
Saez
DE
, et al
.
Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations
.
Blood
.
2008
;
111
(
1
):
271
-
274
.
40.
IJspeert
H
,
Driessen
GJ
,
Moorhouse
MJ
, et al
.
Similar recombination-activating gene (RAG) mutations result in similar immunobiological effects but in different clinical phenotypes
.
J Allergy Clin Immunol
.
2014
;
133
(
4
):
1124
-
1133
.
41.
Cassani
B
,
Poliani
PL
,
Marrella
V
, et al
.
Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome
.
J Exp Med
.
2010
;
207
(
7
):
1525
-
1540
.
42.
Meffre
E
.
The establishment of early B cell tolerance in humans: lessons from primary immunodeficiency diseases
.
Ann N Y Acad Sci
.
2011
;
1246
(
1
):
1
-
10
.
43.
Meffre
E
,
Wardemann
H
.
B-cell tolerance checkpoints in health and autoimmunity
.
Curr Opin Immunol
.
2008
;
20
(
6
):
632
-
638
.
44.
Wang
J
,
Bu
D
,
Zhu
X
.
Immunoglobulin variable region gene analysis to the autoantibody-secreting B cells from tumors in association with paraneoplastic autoimmune multiorgan syndrome
.
Int J Dermatol
.
2007
;
46
(
11
):
1146
-
1154
.
45.
Pascual
V
,
Victor
K
,
Lelsz
D
, et al
.
Nucleotide sequence analysis of the V regions of two IgM cold agglutinins. Evidence that the VH4-21 gene segment is responsible for the major cross-reactive idiotype
.
J Immunol
.
1991
;
146
(
12
):
4385
-
4391
.
46.
Lee
YN
,
Frugoni
F
,
Dobbs
K
, et al
.
Characterization of T and B cell repertoire diversity in patients with RAG deficiency
.
Sci Immunol
.
2016
;
1
(
6
):
eaah6109
.
47.
Manichanh
C
,
Borruel
N
,
Casellas
F
,
Guarner
F
.
The gut microbiota in IBD
.
Nat Rev Gastroenterol Hepatol
.
2012
;
9
(
10
):
599
-
608
.
48.
Pellicciotta
M
,
Rigoni
R
,
Falcone
EL
,
Holland
SM
,
Villa
A
,
Cassani
B
.
The microbiome and immunodeficiencies: lessons from rare diseases
.
J Autoimmun
.
2019
;
98
:
132
-
148
.
49.
Mitra
A
,
Pollock
B
,
Gooi
J
,
Darling
JC
,
Boon
A
,
Newton-Bishop
JA
.
Cutaneous granulomas associated with primary immunodeficiency disorders
.
Br J Dermatol
.
2005
;
153
(
1
):
194
-
199
.
50.
Neven
B
,
Pérot
P
,
Bruneau
J
, et al
.
Cutaneous and visceral chronic granulomatous disease triggered by a rubella virus vaccine strain in children with primary immunodeficiencies
.
Clin Infect Dis
.
2017
;
64
(
1
):
83
-
86
.
51.
Dutmer
CM
,
Asturias
EJ
,
Smith
C
, et al
.
Late onset hypomorphic RAG2 deficiency presentation with fatal vaccine-strain VZV infection
.
J Clin Immunol
.
2015
;
35
(
8
):
754
-
760
.
52.
Perelygina
L
,
Plotkin
S
,
Russo
P
, et al
.
Rubella persistence in epidermal keratinocytes and granuloma M2 macrophages in patients with primary immunodeficiencies
.
J Allergy Clin Immunol
.
2016
;
138
(
5
):
1436
-
1439.e1
.
53.
Buchbinder
D
,
Hauck
F
,
Albert
MH
, et al
.
Rubella virus-associated cutaneous granulomatous disease: a unique complication in immune-deficient patients, not limited to DNA repair disorders
.
J Clin Immunol
.
2019
;
39
(
1
):
81
-
89
.
54.
Klein
L
,
Kyewski
B
,
Allen
PM
,
Hogquist
KA
.
Positive and negative selection of the T cell repertoire: what thymocytes see (and don’t see)
.
Nat Rev Immunol
.
2014
;
14
(
6
):
377
-
391
.
55.
Stritesky
GL
,
Jameson
SC
,
Hogquist
KA
.
Selection of self-reactive T cells in the thymus
.
Annu Rev Immunol
.
2012
;
30
(
1
):
95
-
114
.
56.
Owen
DL
,
Mahmud
SA
,
Sjaastad
LE
, et al
.
Thymic regulatory T cells arise via two distinct developmental programs
.
Nat Immunol
.
2019
;
20
(
2
):
195
-
205
.
57.
Arnaiz-Villena
A
,
Timon
M
,
Corell
A
,
Perez-Aciego
P
,
Martin-Villa
JM
,
Regueiro
JR
.
Brief report: primary immunodeficiency caused by mutations in the gene encoding the CD3-gamma subunit of the T-lymphocyte receptor
.
N Engl J Med
.
1992
;
327
(
8
):
529
-
533
.
58.
Tokgoz
H
,
Caliskan
U
,
Keles
S
,
Reisli
I
,
Guiu
IS
,
Morgan
NV
.
Variable presentation of primary immune deficiency: two cases with CD3 gamma deficiency presenting with only autoimmunity
.
Pediatr Allergy Immunol
.
2013
;
24
(
3
):
257
-
262
.
59.
Rowe
JH
,
Delmonte
OM
,
Keles
S
, et al
.
Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function
.
Blood
.
2018
;
131
(
21
):
2335
-
2344
.
60.
Turul
T
,
Tezcan
I
,
Artac
H
, et al
.
Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency
.
Eur J Pediatr
.
2009
;
168
(
1
):
87
-
93
.
61.
Liu
Q
,
Wang
YP
,
Liu
Q
, et al
.
Novel compound heterozygous mutations in ZAP70 in a Chinese patient with leaky severe combined immunodeficiency disorder
.
Immunogenetics
.
2017
;
69
(
4
):
199
-
209
.
62.
Chan
AY
,
Punwani
D
,
Kadlecek
TA
, et al
.
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70
.
J Exp Med
.
2016
;
213
(
2
):
155
-
165
.
63.
Keller
B
,
Zaidman
I
,
Yousefi
OS
, et al
.
Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT
.
J Exp Med
.
2016
;
213
(
7
):
1185
-
1199
.
64.
Hauck
F
,
Randriamampita
C
,
Martin
E
, et al
.
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency
.
J Allergy Clin Immunol
.
2012
;
130
(
5
):
1144
-
1152.e11
.
65.
Turvey
SE
,
Durandy
A
,
Fischer
A
, et al
.
The CARD11-BCL10-MALT1 (CBM) signalosome complex: stepping into the limelight of human primary immunodeficiency
.
J Allergy Clin Immunol
.
2014
;
134
(
2
):
276
-
284
.
66.
Blonska
M
,
Lin
X
.
CARMA1-mediated NF-kappaB and JNK activation in lymphocytes
.
Immunol Rev
.
2009
;
228
(
1
):
199
-
211
.
67.
Shinohara
H
,
Yasuda
T
,
Aiba
Y
, et al
.
PKC beta regulates BCR-mediated IKK activation by facilitating the interaction between TAK1 and CARMA1
.
J Exp Med
.
2005
;
202
(
10
):
1423
-
1431
.
68.
Thome
M
,
Charton
JE
,
Pelzer
C
,
Hailfinger
S
.
Antigen receptor signaling to NF-kappaB via CARMA1, BCL10, and MALT1
.
Cold Spring Harb Perspect Biol
.
2010
;
2
(
9
):
a003004
.
69.
Hamilton
KS
,
Phong
B
,
Corey
C
, et al
.
T cell receptor-dependent activation of mTOR signaling in T cells is mediated by Carma1 and MALT1, but not Bcl10
.
Sci Signal
.
2014
;
7
(
329
):
ra55
.
70.
Lu
HY
,
Bauman
BM
,
Arjunaraja
S
, et al
.
The CBM-opathies - a rapidly expanding spectrum of human inborn errors of immunity caused by mutations in the CARD11-BCL10-MALT1 complex
.
Front Immunol
.
2018
;
9
:
2078
.
71.
Fuchs
S
,
Rensing-Ehl
A
,
Pannicke
U
, et al
.
Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency
.
Blood
.
2015
;
126
(
14
):
1658
-
1669
.
72.
Ma
CA
,
Stinson
JR
,
Zhang
Y
, et al
.
Germline hypomorphic CARD11 mutations in severe atopic disease [published correction appear in Nat Genet. 2017;49(11):1161]
.
Nat Genet
.
2017
;
49
(
8
):
1192
-
1201
.
73.
Dadi
H
,
Jones
TA
,
Merico
D
, et al
.
Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11)
.
J Allergy Clin Immunol
.
2018
;
141
(
5
):
1818
-
1830.e2
.
74.
Jabara
HH
,
Ohsumi
T
,
Chou
J
, et al
.
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiency
.
J Allergy Clin Immunol
.
2013
;
132
(
1
):
151
-
158
.
75.
McKinnon
ML
,
Rozmus
J
,
Fung
SY
, et al
.
Combined immunodeficiency associated with homozygous MALT1 mutations
.
J Allergy Clin Immunol
.
2014
;
133
(
5
):
1458
-
1462
,
1462.e1-7
.
76.
Charbit-Henrion
F
,
Jeverica
AK
,
Bègue
B
, et al;
GENIUS Group
.
Deficiency in mucosa-associated lymphoid tissue lymphoma translocation 1: a novel cause of IPEX-like syndrome
.
J Pediatr Gastroenterol Nutr
.
2017
;
64
(
3
):
378
-
384
.
77.
Bornancin
F
,
Renner
F
,
Touil
R
, et al
.
Deficiency of MALT1 paracaspase activity results in unbalanced regulatory and effector T and B cell responses leading to multiorgan inflammation
.
J Immunol
.
2015
;
194
(
8
):
3723
-
3734
.
78.
Laman
JD
,
Claassen
E
,
Noelle
RJ
.
Functions of CD40 and its ligand, gp39 (CD40L)
.
Crit Rev Immunol
.
2017
;
37
(
2-6
):
371
-
420
.
79.
Henn
V
,
Slupsky
JR
,
Gräfe
M
, et al
.
CD40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells
.
Nature
.
1998
;
391
(
6667
):
591
-
594
.
80.
França
TT
,
Barreiros
LA
,
Al-Ramadi
BK
,
Ochs
HD
,
Cabral-Marques
O
,
Condino-Neto
A
.
CD40 ligand deficiency: treatment strategies and novel therapeutic perspectives
.
Expert Rev Clin Immunol
.
2019
;
15
(
5
):
529
-
540
.
81.
Hayward
AR
,
Levy
J
,
Facchetti
F
, et al
.
Cholangiopathy and tumors of the pancreas, liver, and biliary tree in boys with X-linked immunodeficiency with hyper-IgM
.
J Immunol
.
1997
;
158
(
2
):
977
-
983
.
82.
Stephens
J
,
Cosyns
M
,
Jones
M
,
Hayward
A
.
Liver and bile duct pathology following Cryptosporidium parvum infection of immunodeficient mice
.
Hepatology
.
1999
;
30
(
1
):
27
-
35
.
83.
Levy
J
,
Espanol-Boren
T
,
Thomas
C
, et al
.
Clinical spectrum of X-linked hyper-IgM syndrome
.
J Pediatr
.
1997
;
131
(
1 Pt 1
):
47
-
54
.
84.
Winkelstein
JA
,
Marino
MC
,
Ochs
H
, et al
.
The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients
.
Medicine (Baltimore)
.
2003
;
82
(
6
):
373
-
384
.
85.
Cabral-Marques
O
,
Klaver
S
,
Schimke
LF
, et al
.
First report of the hyper-IgM syndrome registry of the Latin American Society for Immunodeficiencies: novel mutations, unique infections, and outcomes
.
J Clin Immunol
.
2014
;
34
(
2
):
146
-
156
.
86.
Leven
EA
,
Maffucci
P
,
Ochs
HD
, et al
.
Hyper IgM syndrome: a report from the USIDNET Registry
.
J Clin Immunol
.
2016
;
36
(
5
):
490
-
501
.
87.
Hirbod-Mobarakeh
A
,
Aghamohammadi
A
,
Rezaei
N
.
Immunoglobulin class switch recombination deficiency type 1 or CD40 ligand deficiency: from bedside to bench and back again
.
Expert Rev Clin Immunol
.
2014
;
10
(
1
):
91
-
105
.
88.
Lacroix-Desmazes
S
,
Resnick
I
,
Stahl
D
, et al
.
Defective self-reactive antibody repertoire of serum IgM in patients with hyper-IgM syndrome
.
J Immunol
.
1999
;
162
(
9
):
5601
-
5608
.
89.
Cicalese
MP
,
Gerosa
J
,
Baronio
M
, et al
.
Circulating follicular helper and follicular regulatory T cells are severely compromised in human CD40 deficiency: a case report
.
Front Immunol
.
2018
;
9
:
1761
.
90.
Quartier
P
,
Bustamante
J
,
Sanal
O
, et al
.
Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to activation-induced cytidine deaminase deficiency
.
Clin Immunol
.
2004
;
110
(
1
):
22
-
29
.
91.
Cantaert
T
,
Schickel
JN
,
Bannock
JM
, et al
.
Activation-induced cytidine deaminase expression in human B cell precursors is essential for central B cell tolerance
.
Immunity
.
2015
;
43
(
5
):
884
-
895
.
92.
Cantaert
T
,
Schickel
JN
,
Bannock
JM
, et al
.
Decreased somatic hypermutation induces an impaired peripheral B cell tolerance checkpoint
.
J Clin Invest
.
2016
;
126
(
11
):
4289
-
4302
.
93.
Hanna
S
,
Etzioni
A
.
MHC class I and II deficiencies
.
J Allergy Clin Immunol
.
2014
;
134
(
2
):
269
-
275
.
94.
Moins-Teisserenc
HT
,
Gadola
SD
,
Cella
M
, et al
.
Association of a syndrome resembling Wegener’s granulomatosis with low surface expression of HLA class-I molecules [published correction appears in Lancet. 2000;356(9224):170]
.
Lancet
.
1999
;
354
(
9190
):
1598
-
1603
.
95.
Gadola
SD
,
Moins-Teisserenc
HT
,
Trowsdale
J
,
Gross
WL
,
Cerundolo
V
.
TAP deficiency syndrome
.
Clin Exp Immunol
.
2000
;
121
(
2
):
173
-
178
.
96.
Marcus
N
,
Stauber
T
,
Lev
A
, et al
.
MHC II deficient infant identified by newborn screening program for SCID
.
Immunol Res
.
2018
;
66
(
4
):
537
-
542
.
97.
Lev
A
,
Simon
AJ
,
Broides
A
, et al
.
Thymic function in MHC class II-deficient patients
.
J Allergy Clin Immunol
.
2013
;
131
(
3
):
831
-
839
.
98.
Abdollahpour
H
,
Appaswamy
G
,
Kotlarz
D
, et al
.
The phenotype of human STK4 deficiency
.
Blood
.
2012
;
119
(
15
):
3450
-
3457
.
99.
Nehme
NT
,
Schmid
JP
,
Debeurme
F
, et al
.
MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival
.
Blood
.
2012
;
119
(
15
):
3458
-
3468
.
100.
Halacli
SO
,
Ayvaz
DC
,
Sun-Tan
C
, et al
.
STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: a novel mutation
.
Clin Immunol
.
2015
;
161
(
2
):
316
-
323
.
101.
Schipp
C
,
Schlütermann
D
,
Hönscheid
A
, et al
.
EBV negative lymphoma and autoimmune lymphoproliferative syndrome like phenotype extend the clinical spectrum of primary immunodeficiency caused by STK4 deficiency
.
Front Immunol
.
2018
;
9
:
2400
.
102.
Moran
I
,
Avery
DT
,
Payne
K
, et al;
CIRCA
.
B cell-intrinsic requirement for STK4 in humoral immunity in mice and human subjects
.
J Allergy Clin Immunol
.
2019
;
143
(
6
):
2302
-
2305
.
103.
Spolski
R
,
Gromer
D
,
Leonard
WJ
.
The γ c family of cytokines: fine-tuning signals from IL-2 and IL-21 in the regulation of the immune response
.
F1000 Res
.
2017
;
6
:
1872
.
104.
Yoshizaki
A
,
Miyagaki
T
,
DiLillo
DJ
, et al
.
Regulatory B cells control T-cell autoimmunity through IL-21-dependent cognate interactions
.
Nature
.
2012
;
491
(
7423
):
264
-
268
.
105.
Salzer
E
,
Kansu
A
,
Sic
H
, et al
.
Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency
.
J Allergy Clin Immunol
.
2014
;
133
(
6
):
1651
-
1659.e12
.
106.
Kotlarz
D
,
Ziętara
N
,
Uzel
G
, et al
.
Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome
.
J Exp Med
.
2013
;
210
(
3
):
433
-
443
.
107.
Erman
B
,
Bilic
I
,
Hirschmugl
T
, et al
.
Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R
.
Haematologica
.
2015
;
100
(
6
):
e216
-
e219
.
108.
Wang
Y
,
Jiang
X
,
Zhu
J
, et al
.
IL-21/IL-21R signaling suppresses intestinal inflammation induced by DSS through regulation of Th responses in lamina propria in mice
.
Sci Rep
.
2016
;
6
(
1
):
31881
.
109.
Sharpe
AH
,
Freeman
GJ
.
The B7-CD28 superfamily
.
Nat Rev Immunol
.
2002
;
2
(
2
):
116
-
126
.
110.
Xu
H
,
Li
X
,
Liu
D
, et al
.
Follicular T-helper cell recruitment governed by bystander B cells and ICOS-driven motility
.
Nature
.
2013
;
496
(
7446
):
523
-
527
.
111.
Landuyt
AE
,
Klocke
BJ
,
Colvin
TB
,
Schoeb
TR
,
Maynard
CL
.
Cutting edge: ICOS-deficient regulatory T cells display normal induction of Il10 but readily downregulate expression of Foxp3
.
J Immunol
.
2019
;
202
(
4
):
1039
-
1044
.
112.
Grimbacher
B
,
Hutloff
A
,
Schlesier
M
, et al
.
Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency
.
Nat Immunol
.
2003
;
4
(
3
):
261
-
268
.
113.
Schepp
J
,
Chou
J
,
Skrabl-Baumgartner
A
, et al
.
14 years after discovery: clinical follow-up on 15 patients with inducible co-stimulator deficiency
.
Front Immunol
.
2017
;
8
:
964
.
114.
Takahashi
N
,
Matsumoto
K
,
Saito
H
, et al
.
Impaired CD4 and CD8 effector function and decreased memory T cell populations in ICOS-deficient patients
.
J Immunol
.
2009
;
182
(
9
):
5515
-
5527
.
115.
Ito
T
,
Yang
M
,
Wang
YH
, et al
.
Plasmacytoid dendritic cells prime IL-10-producing T regulatory cells by inducible costimulator ligand
.
J Exp Med
.
2007
;
204
(
1
):
105
-
115
.
116.
Nunes-Santos
CJ
,
Uzel
G
,
Rosenzweig
SD
.
PI3K pathway defects leading to immunodeficiency and immune dysregulation
.
J Allergy Clin Immunol
.
2019
;
143
(
5
):
1676
-
1687
.
117.
Notarangelo
LD
,
Fleisher
TA
.
Targeted strategies directed at the molecular defect: Toward precision medicine for select primary immunodeficiency disorders
.
J Allergy Clin Immunol
.
2017
;
139
(
3
):
715
-
723
.
118.
Maccari
ME
,
Abolhassani
H
,
Aghamohammadi
A
, et al
.
Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase δ syndrome: the European Society for Immunodeficiencies-activated phosphoinositide 3-kinase δ syndrome registry
.
Front Immunol
.
2018
;
9
:
543
.
119.
Nademi
Z
,
Slatter
MA
,
Dvorak
CC
, et al
.
Hematopoietic stem cell transplant in patients with activated PI3K delta syndrome
.
J Allergy Clin Immunol
.
2017
;
139
(
3
):
1046
-
1049
.
120.
Okano
T
,
Imai
K
,
Tsujita
Y
, et al
.
Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 1
.
J Allergy Clin Immunol
.
2019
;
143
(
1
):
266
-
275
.
121.
Rao
VK
,
Webster
S
,
Dalm
VASH
, et al
.
Effective “activated PI3Kδ syndrome”-targeted therapy with the PI3Kδ inhibitor leniolisib
.
Blood
.
2017
;
130
(
21
):
2307
-
2316
.
Sign in via your Institution