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

Irina Zaretsky, Ofir Atrakchi, Roei D. Mazor, Liat Stoler-Barak, Adi Biram, Sara W. Feigelson, Alexander D. Gitlin, Britta Engelhardt, Ziv Shulman

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Pages (from-to)3435-3448
Number of pages14
JournalJournal of Experimental Medicine
Volume214
Issue number11
DOIs
StatePublished - 1 Nov 2017

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology

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