Prolonged circulation of immune complexes due to various altered immune functions contributes to nephritis in MRL/lpr mice.

Abstract:

:To gain some insight into the pathogenesis of proliferative lupus nephritis in MRL/lpr mice we investigated the kinetics of removal of immune complexes from the circulation, the carrier state of blood cells, the uptake of complexes by the mononuclear phagocyte system, and the localization of complexes in kidneys. In nephritic MRL/lpr mice challenged with a subsaturating dose of radiolabelled complexes (2.5 mg bovine serum albumin-anti-bovine serum albumin) liver uptake was profoundly decreased, removal of circulating complexes was delayed, and 12-h kidney localization of complexes was enhanced 7.3-fold, in comparison to control mice. The findings were not encumbered by differences in complement concentration and most likely are attributable to various altered immune functions: spontaneous polyclonal activation of B cells, enhanced production of endogenous immune complexes, delayed removal of complexes from the circulation, and decreased uptake of complexes by the mononuclear phagocyte system. In concert, such altered functions contribute to prolonged circulation of complexes to result in their enhanced deposition in the microcirculation.

journal_name

Clin Exp Immunol

authors

Granholm NA,Cavallo T

doi

10.1111/j.1365-2249.1990.tb05443.x

subject

Has Abstract

pub_date

1990-11-01 00:00:00

pages

300-6

issue

2

eissn

0009-9104

issn

1365-2249

journal_volume

82

pub_type

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