| First Author | Deobagkar-Lele M | Year | 2024 |
| Journal | Sci Immunol | Volume | 9 |
| Issue | 98 | Pages | eadd4874 |
| PubMed ID | 39121196 | Mgi Jnum | J:362924 |
| Mgi Id | MGI:7782822 | Doi | 10.1126/sciimmunol.add4874 |
| Citation | Deobagkar-Lele M, et al. (2024) B cells require DOCK8 to elicit and integrate T cell help when antigen is limiting. Sci Immunol 9(98):eadd4874 |
| abstractText | 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. |
