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Possible Role of Natural Immune Response against Altered Fibroblasts in the Development of Post‐Operative Adhesions
Author(s) -
Alpay Zeynep,
Özgönenel Melike S.,
Savaşan Süreyya,
Buck Steven,
Saed Ghassan M.,
Diamond Michael P.
Publication year - 2006
Publication title -
american journal of reproductive immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 97
eISSN - 1600-0897
pISSN - 1046-7408
DOI - 10.1111/j.1600-0897.2006.00378.x
Subject(s) - immune system , fibroblast , immunology , lymphokine , lymphocyte , biology , lymphokine activated killer cell , flow cytometry , mixed lymphocyte reaction , cell , t cell , chemistry , microbiology and biotechnology , in vitro , interleukin 21 , biochemistry
Problem Post‐operative adhesion tissue fibroblasts (ATF) differ from normal peritoneal fibroblasts (NPF). Natural immune response participates in the elimination of altered cells. In this study, we investigated NPF and ATF expression patterns of immune response‐related markers, and lymphokine‐activated killer (LAK) cell‐mediated fibroblast elimination in vitro . Method of study Primary cell cultures of both NPF and ATF obtained from the same four patients were used in the experiments. The expression of CD54, CD40 and CD120b, and allogeneic LAK cell‐mediated ATF and NPF elimination were studied by flow cytometry. Results Average expression of CD54 in ATF was greater by 12.3‐fold compared with NPF ( P = 0.021), with ratios of 2.4 and 1.9‐fold for CD40 ( P < 0.001) and CD120b ( P = 0.013), respectively. Average LAK cell‐mediated fibroblast killing was 1.8 ± 0.8‐fold greater in ATF over NPF ( P = 0.008). Furthermore, LAK cell‐mediated fibroblast elimination correlated significantly with the increased CD40, CD54 and CD120b expression ( R > 0.956; P < 0.05 for each). Conclusions These results demonstrate that ATF are more susceptible to lymphocyte‐mediated elimination than NPF and the development of adhesions despite this could be explained by either impaired or overwhelmed autologous natural immune response against reactive fibroblasts.