Correlation of alternative pathway (AP) lytic activity and AP-dependent neutrophil phagocytosis with factor B levels and consumption in serum

Citation
Ai. Assis-pandochi et al., Correlation of alternative pathway (AP) lytic activity and AP-dependent neutrophil phagocytosis with factor B levels and consumption in serum, IMMUNOL INV, 28(5-6), 1999, pp. 311-321
Citations number
26
Categorie Soggetti
Immunology
Journal title
IMMUNOLOGICAL INVESTIGATIONS
ISSN journal
08820139 → ACNP
Volume
28
Issue
5-6
Year of publication
1999
Pages
311 - 321
Database
ISI
SICI code
0882-0139(1999)28:5-6<311:COAP(L>2.0.ZU;2-H
Abstract
This work investigated the correlation between serum levels of factor B, AP -lytic activity, ratio of factor B activation by zymosan, and AP-dependent neutrophil phagocytosis in samples of normal human serum (NHS). In addition , since the antithyroid drug propylthiouracil (PTU) induces increased level s of AP lytic activity in rats, groups of these animals were treated with t his drug in order to increase AP titers and to evaluate those parameters al so in this condition. The results showed no correlation between factor B co ncentration and AP lytic activity in 18 samples of NHS or between factor B concentration and proportion of consumption by zymosan. Interestingly, this consumption was also not correlated with phagocytosis as measured by the c hemiluminescence (CL) response of neutrophils to the opsonized particles. T he two biological properties of phagocytosis and lytic activity, dependent of AP, were not correlated to each other in the NHS samples. In the samples of rat serum with increased AP lytic levels a different result was observe d. A positive correlation between CL response and lytic activity occurred i n serum of animals receiving a low PTU dose, but not in serum of animals re ceiving a high dose, where CL responses were lower than those of controls. The results are compared to literature data and discussed in terms of indiv idual differences in resistance or susceptibility to infections and or dise ases involving the complement system.