The iNKT cell represents a novel therapeutic target for important hematologic diseases such as sickle cell disease (SCD) and myeloma. While an antibody specifically targeting human iNKT cells is now in a clinical trial, no surrogate reagent that specifically recognizes murine iNKT cells has been previously reported. This abstract defines work on a unique, recently developed antibody specifically directed to the T cell receptor of the mouse iNKT cell. These cells are a small subset of T lymphocytes that share characteristics with adaptive as well as innate immune cells. In contrast to conventional T cells they recognize glycolipid antigens presented on the MHC-I like molecule CD1d. Upon activation they can rapidly release either pro-inflammatory or anti-inflammatory cytokines, depending on stimulus and microenvironment. This enables them to direct downstream immune functions into inflammatory or tolerizing modes. iNKT cell activation has been implicated as a mediator of the chronic inflammation that is found in patients with SCD (Field et al. Blood 121:3321, 2013) suggesting that reduction of activity or iNKT cell depletion may be an effective therapy. The activation of iNKT cells has been shown to have therapeutics effects in multiple hematologic tumors including myeloma, lymphoma, and leukemia (Dhodapkar and Richter Clin.Immunol.140:160, 2011). Until now, the role of iNKT cells in immune regulation has been studied using iNKT cell deficient inbred mouse strains like CD1d and Ja18 knockout mice or with the iNKT cell activating agent alpha-Galactosyl-Ceramide (aGalCer). These tools have weaknesses and limitations. CD1d deficient mice are not only deficient in invariant NKT cells but also other CD1d restricted cells, such as Type 2 NKT cells. Ja18 knockout mice have recently been shown to have a substantial decrease in TCR diversity in addition to their iNKT cell deficiency (Bedel et al.,Nat Immunol. 2012 Jul 19;13(8):705-6.). Furthermore, these mouse strains lack iNKT cells from birth and little is known about pharmacologic suppression in iNKT cell competent mouse strains. Although aGalCer can be used to activate iNKT cells in vivo, it induces a persistent iNKT cell anergy after activation. NKT Therapeutics has developed human iNKT cell specific humanized monoclonal antibodies, one of which is currently being evaluated in a Phase I study in patients with sickle cell disease. The human iNKT cell specific antibodies are not cross-reactive to murine iNKT cells. In order to better understand the potential of pharmacologic modulation of iNKT cell function in pre-clinical disease models, we developed a mouse iNKT specific monoclonal antibody. We have a generated both a depleting version (NKT-14) and by manipulating the FC-function through mutations we have also generated a non-depleting, activating version (NKT-14m). Both are highly specific for mouse iNKT cells and recognize all aGalCer -loaded CD1d tetramer binding cells (Fig. 1A) in multiple inbred mouse strains tested (C57BL/6, BALB/c, NOD, DBA, C3H,NZW, NZW/NZB F1, AKR, SJL and A/J). NKT-14 rapidly and very specifically depletes iNKT cells in vivo (Fig. 1B). NKT-14m can activate iNKT cells in vivo and induces release if IFn-Gamma (Fig. 1C). These novel mouse invariant TCR specific monoclonal antibodies will allow us to better understand the role of iNKT cells in health and disease in order to inform clinical trials of therapeutics which manipulate these unique immune regulatory cells for the treatment of disease.

Figure 1
Figure 1. A C57BL/6 splenocytes were stained with NKT14 or isotype control followed by a secondary anti mouse IgG2a monoclonal and aGalCer loaded CD1d Tetramer. B C57BL/6 mice were injected with 50 µg NKT14 or isotype control. Mice were sacrifice 24 hours after dosing and splenocytes prepared, counted and stained for CD3, CD4, CD8 and aGalCer loaded CD1d Tetramer to assess specifity of iNKT cell depletion. C C57BL/6 mice were injected with 2µg aGalCer, 50 µg NKT14m or isotype control. 2 hours post dosing mice were sacrificed, splenocytes prepared and stained for CD3 and aGalCer loaded CD1d tetramers to identify iNKT cells, washed, fixed, permeabilized and stained for intracellular IFn-Gamma.
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A C57BL/6 splenocytes were stained with NKT14 or isotype control followed by a secondary anti mouse IgG2a monoclonal and aGalCer loaded CD1d Tetramer. B C57BL/6 mice were injected with 50 µg NKT14 or isotype control. Mice were sacrifice 24 hours after dosing and splenocytes prepared, counted and stained for CD3, CD4, CD8 and aGalCer loaded CD1d Tetramer to assess specifity of iNKT cell depletion. C C57BL/6 mice were injected with 2µg aGalCer, 50 µg NKT14m or isotype control. 2 hours post dosing mice were sacrificed, splenocytes prepared and stained for CD3 and aGalCer loaded CD1d tetramers to identify iNKT cells, washed, fixed, permeabilized and stained for intracellular IFn-Gamma.

Figure 1
Figure 1. A C57BL/6 splenocytes were stained with NKT14 or isotype control followed by a secondary anti mouse IgG2a monoclonal and aGalCer loaded CD1d Tetramer. B C57BL/6 mice were injected with 50 µg NKT14 or isotype control. Mice were sacrifice 24 hours after dosing and splenocytes prepared, counted and stained for CD3, CD4, CD8 and aGalCer loaded CD1d Tetramer to assess specifity of iNKT cell depletion. C C57BL/6 mice were injected with 2µg aGalCer, 50 µg NKT14m or isotype control. 2 hours post dosing mice were sacrificed, splenocytes prepared and stained for CD3 and aGalCer loaded CD1d tetramers to identify iNKT cells, washed, fixed, permeabilized and stained for intracellular IFn-Gamma.
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A C57BL/6 splenocytes were stained with NKT14 or isotype control followed by a secondary anti mouse IgG2a monoclonal and aGalCer loaded CD1d Tetramer. B C57BL/6 mice were injected with 50 µg NKT14 or isotype control. Mice were sacrifice 24 hours after dosing and splenocytes prepared, counted and stained for CD3, CD4, CD8 and aGalCer loaded CD1d Tetramer to assess specifity of iNKT cell depletion. C C57BL/6 mice were injected with 2µg aGalCer, 50 µg NKT14m or isotype control. 2 hours post dosing mice were sacrificed, splenocytes prepared and stained for CD3 and aGalCer loaded CD1d tetramers to identify iNKT cells, washed, fixed, permeabilized and stained for intracellular IFn-Gamma.

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Disclosures:

Scheuplein:NKT Therapeutics: Employment. Thariath:NKT Therapeutics: Employment. Mashal:NKT Therapeutics: Employment, Equity Ownership. Schaub:NKT Therapeutics: Employment.

Topics:
mice, monoclonal antibodies, natural killer t-cells, immunoglobulin isotypes, antibodies, blood cell depletion therapy, interferon type ii, multiple myeloma, sickle cell anemia, antigens

Author notes

*

Asterisk with author names denotes non-ASH members.

© 2013 by The American Society of Hematology
2013
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