Enhanced B cell immune responses in humanized γδ TCR mice post antigens immunization 2643

Abstract Description The humanized gamma delta (γδ) T cell receptor (TCR) mouse model represents a pivotal advancement in immunological research, enabling more accurate study of human immune responses. This study evaluates the B cell-mediated immune responses in humanized γδ TCR mice and compared it to wild type (WT) mice after immunization with collagen and keratin immunizations on B cell immune responses in humanized γδ TCR mice and WT mice. Our findings reveal that these immunizations significantly enhance B cell activity in HuTCR mice, as evidenced by increased numbers of antigen-specific antibody-secreting cells (ASCs), elevated antibody titers, and higher percentages of plasma and memory B cells in systemic tissues compared to WT mice. Additionally, we observed pronounced elevated levels of both immunoregulatory and pro-inflammatory cytokines in the serum. These results suggest that γδ TCR signaling plays a critical role in modulating B cell responses, offering new insights into the interplay between γδ T cells and B cells in the context of immunization. This enhanced understanding of γδ TCR-mediated B cell activation could pave the way for novel immunotherapeutic strategies targeting autoimmune diseases and improving vaccine efficacy. Funding Sources None Topic Categories Translational and Interventional Immunology (TI)

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Publication Details

Journal
The Journal of Immunology
Published
2025-11-01
DOI
https://doi.org/10.1093/jimmun/vkaf283.539
Primary Topic
T-cell and B-cell Immunology
Type
article
Field-Weighted Citation Impact
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article

Enhanced B cell immune responses in humanized γδ TCR mice post antigens immunization 2643

Husheem Michael, Wei He, Gene W. Weng, Wei Weng et al.
The Journal of Immunology
T-cell and B-cell Immunology
article

Enhanced B cell immune responses in humanized γδ TCR mice post antigens immunization 2643

Husheem Michael, Wei He, Gene W. Weng, Wei Weng, Mikaela M. Vallas, Abigail T. Lenihan, Jonathan Barbar
article en

Abstract

Abstract Description The humanized gamma delta (γδ) T cell receptor (TCR) mouse model represents a pivotal advancement in immunological research, enabling more accurate study of human immune responses. This study evaluates the B cell-mediated immune responses in humanized γδ TCR mice and compared it to wild type (WT) mice after immunization with collagen and keratin immunizations on B cell immune responses in humanized γδ TCR mice and WT mice. Our findings reveal that these immunizations significantly enhance B cell activity in HuTCR mice, as evidenced by increased numbers of antigen-specific antibody-secreting cells (ASCs), elevated antibody titers, and higher percentages of plasma and memory B cells in systemic tissues compared to WT mice. Additionally, we observed pronounced elevated levels of both immunoregulatory and pro-inflammatory cytokines in the serum. These results suggest that γδ TCR signaling plays a critical role in modulating B cell responses, offering new insights into the interplay between γδ T cells and B cells in the context of immunization. This enhanced understanding of γδ TCR-mediated B cell activation could pave the way for novel immunotherapeutic strategies targeting autoimmune diseases and improving vaccine efficacy. Funding Sources None Topic Categories Translational and Interventional Immunology (TI)

The Journal of ImmunologyVol. 214(Supplement_1)
Ingenious Targeting Laboratory (United States) (US)
Openalex Percentile: Top 61%
T-cell and B-cell Immunology
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