Author:
Kemp D. J.,Coppel R. L.,Stahl H. D.,Bianco A. E.,Corcoran L. M.,McIntyre P.,Langford C. J.,Favaloro J. M.,Crewther P. E.,Brown G. V.,Mitchell G. F.,Culvenor J. G.,Anders R. F.
Abstract
Sporozoites ofP. falciparumand other Plasmodia appear to be fairly simple antigenically, in that there is a dominant antigen, the circumsporozoite (CS) protein that forms the sporozoite surface coat (Potocnjak, Yoshida, Nussenzweig & Nussensweig, 1980; Santoroet al.1983). Consequently, the CS protein and the gene encoding it have now been studied in considerable detail (Elliset al.1983; Godsonet al.1983; Ozakiet al.1983; Dameet al.1984; Eneaet al.1984). In contrast to sporozoites, the asexual blood stagesof P. falciparumare antigenically complex. Two-dimensional gel analyses of immunoprecipitated, biosynthetically labelled antigens indicate that repeated infection withP. falciparumresults in the synthesis of antibodies against a large number of distinct antigens (Perrin & Dayal, 1982; Brownet al.1981, 1983). In further contrast to the sporozoite, the asexual blood stages of differentP. falciparumisolates exhibit a high degree of antigenic heterogeneity (Brownet al.1983; Hallet al.1983; McBride, Walliker & Morgan, 1982). Much of this antigenic diversity is no doubt due to allelic differences but clonal populations of parasites may also have the capacity to undergo antigenic variation (Hommel, David & Oligino, 1983).
Publisher
Cambridge University Press (CUP)
Subject
Infectious Diseases,Animal Science and Zoology,Parasitology
Cited by
64 articles.
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