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Transmission-Blocking Vaccines: Old Friends and New Prospects
Author(s) -
Festus K. Acquah,
Joshua Adjah,
Kim C. Williamson,
Linda Eva Amoah
Publication year - 2019
Publication title -
infection and immunity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.508
H-Index - 220
eISSN - 1070-6313
pISSN - 0019-9567
DOI - 10.1128/iai.00775-18
Subject(s) - gametocyte , biology , plasmodium falciparum , antigen , virology , midgut , plasmodium (life cycle) , gamete , malaria , parasite hosting , immunology , human fertilization , genetics , ecology , world wide web , computer science , larva
In the progression of the life cycle of Plasmodium falciparum , a small proportion of asexual parasites differentiate into male or female sexual forms called gametocytes. Just like their asexual counterparts, gametocytes are contained within the infected host's erythrocytes (RBCs). However, unlike their asexual partners, they do not exit the RBC until they are taken up in a blood meal by a mosquito. In the mosquito midgut, they are stimulated to emerge from the RBC, undergo fertilization, and ultimately produce tens of thousands of sporozoites that are infectious to humans. This transmission cycle can be blocked by antibodies targeting proteins exposed on the parasite surface in the mosquito midgut, a process that has led to the development of candidate transmission-blocking vaccines (TBV), including some that are in clinical trials. Here we review the leading TBV antigens and highlight the ongoing search for additional gametocyte/gamete surface antigens, as well as antigens on the surfaces of gametocyte-infected erythrocytes, which can potentially become a new group of TBV candidates.

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