Candidate Immediate and Long-term Research Goals: Chandy John is currently a fellow in Pediatric Infectious Diseases/Geographic Medicine at Case Western Reserve University. During the past two years, he has investigated immune responses to the P. falciparum liver-stage antigen-1 in a highland area of Kenya with highly seasonal malaria transmission. His primary areas of interest are the differences in the immune responses of children and adults to P. falciparum antigens and the duration of immune responses to these antigens. The immunological and epidemiologic components of this study represent new approaches for the investigator. Mentored training in these areas will be important to his development as an independent researcher. The proposed study has significant potential for continued future research, specifically comparison of immunity in this area with immunity in a holoendemic area and evaluation of the antigens studied in pilot vaccine trials. The study will provide experience that will enable him to pursue his long-term goal of an academic career with a research focus on the epidemiology of malarial immunity in children and adults. Research Project: Malaria epidemics in highland Kenya may be due in part to prolonged periods of low P. falciparum transmission in the dry season. A consequent decrease in immunologic boosting by P. falciparum antigens may lead to diminished frequencies of the antigen-specific T cells and B cells that maintain partial immunity to malarial infection.
The aims of this project are to determine: 1) whether T and B cell responses to P. falciparum antigens are lower in children than in adults in this area, 2) whether these responses decrease in both children and adults during a period of low transmission, and 3)whether diminished responses correlate with increased susceptibility to infection. Two prospective longitudinal studies will compare antigen-specific T and B cell precursor frequencies and antibody levels in groups of 100 adults and 75 children at times of high and low transmission. The second study will be followed by a treatment/reinfection study. All study subjects will be treated with quinine and sulfadoxime/pyrimethamine, and time to reinfection and level of parasitemia at the time of reinfection will be correlated with duration and level of T and B cell responses. An understanding of the relationship of the duration of immune responses to P. falciparum antigens to susceptibility to infection and disease is important in the evaluation of these antigens as malaria vaccine candidates.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Clinical Investigator Award (CIA) (K08)
Project #
1K08AI001572-01
Application #
2726995
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Program Officer
James, Stephanie
Project Start
1999-09-15
Project End
2003-08-31
Budget Start
1999-09-15
Budget End
2000-08-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Noland, Gregory S; Jansen, Paul; Vulule, John M et al. (2015) Effect of transmission intensity and age on subclass antibody responses to Plasmodium falciparum pre-erythrocytic and blood-stage antigens. Acta Trop 142:47-56
Snider, Cynthia J; Cole, Stephen R; Chelimo, Kiprotich et al. (2012) Recurrent Plasmodium falciparum malaria infections in Kenyan children diminish T-cell immunity to Epstein Barr virus lytic but not latent antigens. PLoS One 7:e31753
Rolfes, Melissa A; McCarra, Matthew; Magak, Ng'wena G et al. (2012) Development of clinical immunity to malaria in highland areas of low and unstable transmission. Am J Trop Med Hyg 87:806-12
Cohen, Justin M; Ernst, Kacey C; Lindblade, Kim A et al. (2010) Local topographic wetness indices predict household malaria risk better than land-use and land-cover in the western Kenya highlands. Malar J 9:328
Moormann, Ann M; Sumba, Peter Odada; Tisch, Daniel J et al. (2009) Stability of interferon-gamma and interleukin-10 responses to Plasmodium falciparum liver stage antigen 1 and thrombospondin-related adhesive protein immunodominant epitopes in a highland population from Western Kenya. Am J Trop Med Hyg 81:489-95
John, Chandy C; Riedesel, Melissa A; Magak, Ng'wena G et al. (2009) Possible interruption of malaria transmission, highland Kenya, 2007-2008. Emerg Infect Dis 15:1917-24
Nguyen, Thanh V; Sacci Jr, John B; de la Vega, Patricia et al. (2009) Characterization of immunoglobulin G antibodies to Plasmodium falciparum sporozoite surface antigen MB2 in malaria exposed individuals. Malar J 8:235
Ernst, Kacey C; Lindblade, Kim A; Koech, David et al. (2009) Environmental, socio-demographic and behavioural determinants of malaria risk in the western Kenyan highlands: a case-control study. Trop Med Int Health 14:1258-65
Menge, David M; Ernst, Kacey C; Vulule, John M et al. (2008) Microscopy underestimates the frequency of Plasmodium falciparum infection in symptomatic individuals in a low transmission highland area. Am J Trop Med Hyg 79:173-7
Cohen, Justin M; Ernst, Kacey C; Lindblade, Kim A et al. (2008) Topography-derived wetness indices are associated with household-level malaria risk in two communities in the western Kenyan highlands. Malar J 7:40

Showing the most recent 10 out of 20 publications