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Polymorphonuclear neutrophils deliver activation signals and antigenic molecules to dendritic cells: a new link between leukocytes upstream of T lymphocytes
Author(s) -
Megiovanni Anna Maria,
Sanchez Françoise,
RobledoSarmiento Macarena,
Morel Céline,
Gluckman Jean Claude,
Boudaly Sarah
Publication year - 2006
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.0905526
Subject(s) - biology , microbiology and biotechnology , cd40 , immunology , cd86 , antigen , immune system , antigen presenting cell , dendritic cell , phagocytosis , t cell , cytotoxic t cell , in vitro , biochemistry
Polymorphonuclear neutrophils (PMNs) are rapidly recruited to tissues upon injury or infection. There, they can encounter local and/or recruited immature dendritic cells (iDCs), a colocalization that could promote at least transient interactions and mutually influence the two leukocyte populations. Using human live blood PMNs and monocyte‐derived iDCs, we examined if these leukocytes actually interacted and whether this influenced DC function. Indeed, coculture with live but not apoptotic PMNs led to up‐regulation of membrane CD40, CD86, and human leukocyte antigen (HLA)‐DR on DCs. Whereas CD40 up‐regulation was dependent on soluble factors released by PMNs, as determined in cultures conducted in different chambers, cell contact was necessary for CD86 and HLA‐DR up‐regulation, a process that was inhibited by anti‐CD18 antibodies, indicating that CD18 ligation was required. We also found that via a cell contact‐dependent mechanism, DCs acquired Candida albicans ‐derived antigens from live as well as from apoptotic PMNs and could thus elicit antigen‐specific T lymphocyte responses. Altogether, our data demonstrate the occurrence of cross‐talk between human PMNs and DCs and provide new insights into the immune processes occurring upstream of the interactions between DCs and T lymphocytes.