Figure 2.
Figure 2. The NPM-ALK transgene can transform normal human CD4+ peripheral T-cells into ALCL. (A) NPM-ALK–transduced normal CD4+ peripheral T cells become immortalized and acquire morphology and surface phenotype of ALCL, including expression of CD30, PD-L1, and IL-10, at least partial loss of the TCR, CD2, CD5, and CD5, and maintenance of CD4. (B) Histologic examination of the tumors formed by the NPM-ALK–transformed CD4+ T cells xenotransplanted into nonobese diabetic/severe combined immunodeficient γ mice reveals their striking and immunophenotypic resemblance to the primary, patient-derived ALK+ ALCL. H&E, hematoxylin and eosin.

The NPM-ALK transgene can transform normal human CD4+peripheral T-cells into ALCL. (A) NPM-ALK–transduced normal CD4+ peripheral T cells become immortalized and acquire morphology and surface phenotype of ALCL, including expression of CD30, PD-L1, and IL-10, at least partial loss of the TCR, CD2, CD5, and CD5, and maintenance of CD4. (B) Histologic examination of the tumors formed by the NPM-ALK–transformed CD4+ T cells xenotransplanted into nonobese diabetic/severe combined immunodeficient γ mice reveals their striking and immunophenotypic resemblance to the primary, patient-derived ALK+ ALCL. H&E, hematoxylin and eosin.

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