In some of the sera from patients with amoebiasis circulating immune complexes are present which are thought to interact with lymphoid cells, enabling them to elicit a burst of oxygen consumption in PMNs. The intensity of chemiluminescence is related to the presence of C3+ and Fc IgG+ cells in the lymphoid cell suspensions employed. The generation and release of highly reactive oxygen derivatives from PMNs impair T lymphocyte proliferative responses to the E. histolytica mitogen. The Authors suggest that one of the mechanisms by which circulating immune complexes present in the sera of patients with amoebiasis may interfere with T cell-mediated immune responses, is through their binding to the surface of the C3+, Fc IgG+ cells with subsequent stimulation of the PMN oxidative metabolism.
Human amoebiasis: the interaction of lymphocyte surface-bound immune complexes and PMNs impairs T cell proliferative responses to E. histolytica mitogen / C. D., Simone; S., Delia; L. D., Meco; Mastroianni, Claudio Maria; C., Mastropietro; Vullo, Vincenzo; F., Sorice. - In: IMMUNOLOGICAL INVESTIGATIONS. - ISSN 0882-0139. - 14:(1985), pp. 131-144.
Human amoebiasis: the interaction of lymphocyte surface-bound immune complexes and PMNs impairs T cell proliferative responses to E. histolytica mitogen.
MASTROIANNI, Claudio Maria;VULLO, Vincenzo;
1985
Abstract
In some of the sera from patients with amoebiasis circulating immune complexes are present which are thought to interact with lymphoid cells, enabling them to elicit a burst of oxygen consumption in PMNs. The intensity of chemiluminescence is related to the presence of C3+ and Fc IgG+ cells in the lymphoid cell suspensions employed. The generation and release of highly reactive oxygen derivatives from PMNs impair T lymphocyte proliferative responses to the E. histolytica mitogen. The Authors suggest that one of the mechanisms by which circulating immune complexes present in the sera of patients with amoebiasis may interfere with T cell-mediated immune responses, is through their binding to the surface of the C3+, Fc IgG+ cells with subsequent stimulation of the PMN oxidative metabolism.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


