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PeerJ. 2017 Jan 10;5:e2855. doi: 10.7717/peerj.2855. eCollection 2017.

Interferon-γ responses to Plasmodium falciparum vaccine candidate antigens decrease in the absence of malaria transmission.

Author information

1
Department of Zoology, Maseno University, Maseno, Kenya.
2
Department of Biological Sciences, Masai Mara University, Narok, Kenya.
3
Department Biological Sciences, Kabianga University, Kericho, Kenya.
4
School of Medicine, Maseno University, Maseno, Kenya.
5
School of Health Sciences, Jaramogi Oginga Odinga University of Science and Technology, Bondo, Kenya.
6
School of Public Health, University of Minnesota, Minneapolis, MN, United States.
7
Medical School, University of Minnesota, Minneapolis, MN, United States.
8
Medical School, Indiana University, Indianapolis, IN, United States.
#
Contributed equally

Abstract

BACKGROUND:

Malaria elimination campaigns are planned or active in many countries. The effects of malaria elimination on immune responses such as antigen-specific IFN- γ responses are not well characterized.

METHODS:

IFN- γ responses to the P. falciparum antigens circumsporozoite protein, liver stage antigen-1, thrombospondin-related adhesive protein, apical membrane antigen-1, MB2, and merozoite surface protein-1 were tested by ELISA in 243 individuals in highland Kenya in April 2008, October 2008, and April 2009, after a one-year period of interrupted malaria transmission from April 2007 to March 2008.

RESULTS:

While one individual (0.4%) tested positive for P. falciparum by PCR inOctober 2008 and another two (0.9%) tested positive in April 2009, no clinical malaria cases were detected during weekly visits. Levels of IFN-γ to all antigens decreased significantly from April 2008 to April 2009 (all P < 0.001).

DISCUSSION:

Naturally acquired IFN- γ responses to P. falciparum antigensare short-lived in the absence of repeated P. falciparum infection. Even short periods of malaria interruption may significantly decrease IFN-γ responses to P. falciparum antigens.

KEYWORDS:

Highland Kenya; Interferon gamma; Malaria; Plasmodium falciparum

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