B cells require DOCK8 to elicit and integrate T cell help when antigen is limiting

Dedicator of cytokinesis 8 (DOCK8) immunodeficiency syndrome is characterized by a failure of the germinal center response, a process involving the proliferation and positive selection of antigen-specific B cells. Here, we describe how DOCK8-deficient B cells are blocked at a light-zone checkpoint in the germinal centers of immunized mice, where they are unable to respond to T cell-dependent survival and selection signals and consequently differentiate into plasma cells or memory B cells. Although DOCK8-deficient B cells can acquire and present antigen to initiate activation of cognate T cells, integrin up-regulation, B cell-T cell conjugate formation, and costimulation are insufficient for sustained B cell and T cell activation when antigen availability is limited. Our findings provide an explanation for the failure of the humoral response in DOCK8 immunodeficiency syndrome and insight into how the level of available antigen modulates B cell-T cell cross-talk to fine-tune humoral immune responses and immunological memory.

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Publication Details

Journal
Science Immunology
Published
2024-08-09
DOI
https://doi.org/10.1126/sciimmunol.add4874
Citations
3
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
0.72

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article

B cells require DOCK8 to elicit and integrate T cell help when antigen is limiting

Rose Hodgson, Aneesha Bhandari, Mukta Deobagkar‐Lele, Tanya L. Crockford et al.
3 citations
Science Immunology
Immunodeficiency and Autoimmune Disorders
0.72
article

B cells require DOCK8 to elicit and integrate T cell help when antigen is limiting

Rose Hodgson, Aneesha Bhandari, Mukta Deobagkar‐Lele, Tanya L. Crockford, Jennifer Back, Katherine R. Bull, Richard J. Cornall, Greg Crawford
article en
3 citations

Abstract

Dedicator of cytokinesis 8 (DOCK8) immunodeficiency syndrome is characterized by a failure of the germinal center response, a process involving the proliferation and positive selection of antigen-specific B cells. Here, we describe how DOCK8-deficient B cells are blocked at a light-zone checkpoint in the germinal centers of immunized mice, where they are unable to respond to T cell-dependent survival and selection signals and consequently differentiate into plasma cells or memory B cells. Although DOCK8-deficient B cells can acquire and present antigen to initiate activation of cognate T cells, integrin up-regulation, B cell-T cell conjugate formation, and costimulation are insufficient for sustained B cell and T cell activation when antigen availability is limited. Our findings provide an explanation for the failure of the humoral response in DOCK8 immunodeficiency syndrome and insight into how the level of available antigen modulates B cell-T cell cross-talk to fine-tune humoral immune responses and immunological memory.

Science ImmunologyVol. 9(98)
Centre for Human Genetics (GB), University of Oxford (GB), MRC Human Immunology Unit (GB), Oxford University Hospitals NHS Trust (GB)
Francis Crick Institute, Kidney Research UK, Medical Research Council
Good health and well-being
Openalex Percentile: Top 29%
Immunodeficiency and Autoimmune Disorders
0.72
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B cells require DOCK8 to elicit and integrate T cell help when antigen is limiting — Rose Hodgson, Aneesha Bhandari, et al. · Science Immunology (2024) | TGRS Research Map | TGRS