Germinal center B cells constitute a predominant physiological source of IL-4: implication for Th2 development in vivo

J Immunol. 2002 Apr 1;168(7):3165-72. doi: 10.4049/jimmunol.168.7.3165.

Abstract

Protective immunity depends upon the capability of the immune system to properly adapt the response to the nature of an infectious agent. CD4(+) Th cells are implicated in this orchestration by secreting a polarized pattern of cytokines. Although Th2 development in animal models and in human cells in vitro to a large extent depends on IL-4, the nature of the cells that provide the initial IL-4 in vivo is still elusive. In this report, we describe the anatomical localization as well as the identity of IL-4-producing cells in human tonsil, a representative secondary lymphoid organ. We demonstrate that IL-4 production is a normal and intrinsic feature of germinal center (GC) B cells. We also show that expression of IL-4 is highly confined to the GCs, in which the B cells constitute the prevalent cellular source. Furthermore, immunofluorescence analysis of colon mucosa reveals a strikingly similar pattern of IL-4-expressing cells compared with tonsils, demonstrating that IL-4 production from GC B cells is not a unique feature of the upper respiratory tract. Our results show that GCs provide the most appropriate microenvironment for IL-4-dependent Th2 polarization in vivo and imply a critical role for GC B cells in this differentiation process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocyte Subsets / immunology*
  • B-Lymphocyte Subsets / metabolism*
  • Cell Differentiation / immunology
  • Cell Separation
  • Cell Survival / immunology
  • Cells, Cultured
  • Colon / cytology
  • Colon / immunology
  • Colon / metabolism
  • Flow Cytometry
  • Germinal Center / cytology*
  • Germinal Center / immunology*
  • Germinal Center / metabolism
  • Humans
  • Immunophenotyping
  • Interleukin-4 / biosynthesis*
  • Interleukin-4 / genetics
  • Interleukin-4 / metabolism
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / metabolism
  • Lymphocyte Count
  • Palatine Tonsil / cytology
  • Palatine Tonsil / immunology
  • Palatine Tonsil / metabolism
  • RNA, Messenger / biosynthesis
  • Th2 Cells / cytology*
  • Th2 Cells / immunology*

Substances

  • RNA, Messenger
  • Interleukin-4