Ex Vivo Cytokine and Memory T Cell Responses to the 42-kDa Fragment ofPlasmodium falciparumMerozoite Surface Protein-1 in Vaccinated Volunteers-Reference-Cited by-同舟云学术

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Ex Vivo Cytokine and Memory T Cell Responses to the 42-kDa Fragment ofPlasmodium falciparumMerozoite Surface Protein-1 in Vaccinated Volunteers

Published:2008-01-21 Issue:3 Volume:180 Page:1451-1461
ISSN:0022-1767
Container-title:The Journal of Immunology
language:en
Short-container-title:J Immunol

Author:

Huaman Maria Cecilia,Martin Laura B.,Malkin Elissa,Narum David L.,Miller Louis H.,Mahanty Siddhartha,Long Carole A.

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

Reference60 articles.

1. Proteolytic processing of thePlasmodium falciparum merozoite surface protein-1 produces a membrane-bound fragment containing two epidermal growth factor-like domains

2. Allelic dimorphism in a surface antigen gene of the malaria parasite Plasmodium falciparum

3. A single fragment of a malaria merozoite surface protein remains on the parasite during red cell invasion and is the target of invasion-inhibiting antibodies.

4. Monoclonal antibodies that inhibit Plasmodium falciparum invasion in vitro recognise the first growth factor-like domain of merozoite surface protein-1

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1. Genetic diversity and natural selection of Plasmodium vivax reticulocyte invasion genes in Ecuador;Malaria Journal;2023-08-03

2. Genetic polymorphism and natural selection in the C-terminal 42 kDa region of merozoite surface protein-1 (MSP-1) among Plasmodium knowlesi samples from Malaysia;Parasites & Vectors;2018-12

3. Down selecting adjuvanted vaccine formulations: a comparative method for harmonized evaluation;BMC Immunology;2018-01-31

4. A chimeric protein-based malaria vaccine candidate induces robust T cell responses against Plasmodium vivax MSP119;Scientific Reports;2016-10-06

5. Rice-produced MSP142ofPlasmodium falciparumelicits antibodies that inhibit parasite growth in vitro;Parasite Immunology;2016-09-29

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