Open AccessCytolytic mechanisms involved in non‐MHC‐restricted cytotoxicity in Chediak‐Higashi syndrome
Author(s) -
Tomoyuki Nakazawa,
Kazunaga Agematsu,
Kozo Yasui,
Takashi Onodera,
Ryosuke Inoue,
Hideo Kaneko,
Naomi Kondo,
Mayu Yamamoto,
Nobuhiko Kayagaki,
Hideo Yagita,
Ko Okumura,
Atsushi Komiyama
Publication year - 1999
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1046/j.1365-2249.1999.01025.x
Subject(s) - chédiak–higashi syndrome , cytolysis , immunology , cytotoxicity , biology , major histocompatibility complex , medicine , immune system , genetics , in vitro
To determine the mechanisms responsible for the impaired lymphocyte‐mediated cytotoxicity in Chediak‐Higashi syndrome (CHS), we investigated the killing ability of peripheral blood lymphocytes (PBL) from three patients with CHS using several kinds of target cells that were sensitive to perforin, Fas ligand (FasL), and/or tumour necrosis factor‐alpha (TNF‐α). Freshly isolated CHS PBL did not kill K562 target cells, killing of which by normal PBL was perforin‐dependent, as demonstrated by complete inhibition by concanamycin A (CMA), an inhibitor of perforin‐based cytotoxicity. In contrast, the CHS PBL exhibited substantial cytotoxicity against Jurkat cells, which was only partially inhibited by CMA treatment but not by the addition of neutralizing anti‐FasL or anti‐TNF‐α antibodies. IL‐2‐activated CHS PBL exhibited substantial levels of cytotoxicity against K562 and Jurkat cells, the levels being 74% and 83% of the respective normal control values, respectively. CMA treatment showed that while the cytotoxicity of IL‐2‐activated CHS PBL against K562 was largely dependent on perforin, that against Jurkat was largely not. IL‐2‐activated CHS PBL expressed FasL mRNA, and killed Fas transfectants. These findings indicate that CHS PBL have an ability to kill some target cells via a perforin‐mediated pathway, especially when they are activated by IL‐2. It was also demonstrated that CHS PBL can exert cytotoxicity against certain target cells by utilizing FasL and an undefined effector molecule other than perforin, FasL, or TNF‐α.