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ICAMs support B cell interactions with T follicular helper cells and promote clonal selection.


ABSTRACT: The germinal center (GC) reaction begins with a diverse and expanded group of B cell clones bearing a wide range of antibody affinities. During GC colonization, B cells engage in long-lasting interactions with T follicular helper (Tfh) cells, a process that depends on antigen uptake and antigen presentation to the Tfh cells. How long-lasting T-B interactions and B cell clonal expansion are regulated by antigen presentation remains unclear. Here, we use in vivo B cell competition models and intravital imaging to examine the adhesive mechanisms governing B cell selection for GC colonization. We find that intercellular adhesion molecule 1 (ICAM-1) and ICAM-2 on B cells are essential for long-lasting cognate Tfh-B cell interactions and efficient selection of low-affinity B cell clones for proliferative clonal expansion. Thus, B cell ICAMs promote efficient antibody immune response by enhancement of T cell help to cognate B cells.

SUBMITTER: Zaretsky I 

PROVIDER: S-EPMC5679169 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

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ICAMs support B cell interactions with T follicular helper cells and promote clonal selection.

Zaretsky Irina I   Atrakchi Ofir O   Mazor Roei D RD   Stoler-Barak Liat L   Biram Adi A   Feigelson Sara W SW   Gitlin Alexander D AD   Engelhardt Britta B   Shulman Ziv Z  

The Journal of experimental medicine 20170922 11


The germinal center (GC) reaction begins with a diverse and expanded group of B cell clones bearing a wide range of antibody affinities. During GC colonization, B cells engage in long-lasting interactions with T follicular helper (Tfh) cells, a process that depends on antigen uptake and antigen presentation to the Tfh cells. How long-lasting T-B interactions and B cell clonal expansion are regulated by antigen presentation remains unclear. Here, we use in vivo B cell competition models and intra  ...[more]

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