Analysis of the Immune Response to the Malaria Parasite in Mali, West Africa

Malaria Clinical Trial

Official title:

Longitudinal Analysis of the B-Cell Immune Response to Plasmodium Falciparum in Mali

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00346346
• Other study ID #: 999906147
• Secondary ID: 06-I-N147
• Status: Completed
• Start date: April 17, 2006
• Est. completion date: January 23, 2013

Study information

• Verified date: January 23, 2013
• Source: National Institutes of Health Clinical Center (CC)
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study will examine the immune response to the malaria parasite at the cellular level to better understand why people achieve natural immunity to the parasite only after multiple infections and why immunity diminishes rapidly in the absence of ongoing infection. The results of this study may provide insight into whether and how natural immunity can be improved upon by vaccination.

Healthy people 2-4 and 18-25 years of age who live in the village of Kambila, Mali, may be eligible for this 1-year study. Participants have a small blood sample collected from a vein in the arm and also from two finger pricks at the beginning of the study, then every 2 months for 6 months and at the end of the study (for a total of five samples). People who become ill with malaria are evaluated and treated by a physician. Those recovering from their first episode of malaria during the study period have another blood sample collection and two finger pricks (bringing to six the total number of samples collected).

Description:

Malaria remains an important public health threat, responsible for over one million deaths annually, the majority among African children. The development of a safe and effective vaccine is widely regarded as a crucial step forward in the control of this disease. However, vaccines tested in clinical trials to date have resulted in very short-lived protection at best. This appears to mirror the kinetics of naturally acquired immunity to Plasmodium falciparum, in that multiple infections are required over many years before clinical immunity is achieved, and then appears to diminish relatively rapidly in the absence of ongoing infection. The mechanisms underlying the delayed acquisition and presumably rapid loss of humoral immunity are poorly understood. A more detailed understanding of these processes on the cellular level may provide insight into whether and how natural immunity can be improved upon by vaccination. This longitudinal cohort study in a P. falciparum endemic village of Mali proposes to test the hypothesis that resistance to malaria is associated with acquisition of P. falciparum specific memory B cells. The 52 week study will cover an entire malaria transmission season and will enroll 224 healthy persons ages 2 to 10 and 18 to 25. After informed consent is obtained from the participant, or the participant's parent or guardian, an age appropriate volume of venous blood will be drawn at baseline, and at 2, 4, 6, and 12 months thereafter; and serum and peripheral blood mononuclear cells (PBMC) will be frozen and stored. One convalescent blood sample per participant will also be drawn within two weeks of their first symptomatic P. falciparum infection. Clinical data, including the frequency and severity of malaria infections, will be collected during the study period by passive surveillance. After 52 weeks, serum and PBMC will be thawed and analyzed to determine antibody titers to malaria antigens and to enumerate relevant B cell subpopulations, including total and antigen-specific naive, memory, and plasma cells by ELISPOT assays and flow cytometry.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 237
• Est. completion date: January 23, 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 25 Years

Eligibility

• INCLUSION CRITERIA - HEALTHY VOLUNTEERS AT ENROLLMENT:

1. Males and females ages 2 to 10 years or 18 to 25 years.

2. Will be living in Kambila for one year and available for 12 month follow-up.

3. Willing to have blood specimens stored.

4. Willingness of adult volunteer to participate in the study as evidenced by the completed informed consent document.

5. Willingness of parent or guardian to have his or her child participate in the study as evidenced by the completed informed consent document.

EXCLUSION CRITERIA - HEALTHY VOLUNTEERS AT ENROLLMENT:

1. Active bleeding or hematocrit less than or equal to 15 % (for both children and adults).

2. Fever greater than 38 degrees C, or systemic illness at enrollment.

3. Currently using anti-malarial medications.

4. The following two exclusion items may not have occurred in the last 30 days:

participation in a vaccine or drug trial, or use of corticosteroid or other immunosuppressive drugs.

5. Current pregnancy or a plan to become pregnant during the one year study period. Pregnancy status will be determined at enrollment by urine dipstick, and at subsequent time points by self-report only.

6. While on this protocol, if a subject enrolls in another study that requires the administration of experimental therapies (vaccines or medications), he/she may no longer participate in this protocol.

(Presence of P. falciparum parasitemia in the absence of symptoms at the time of screening is not exclusionary).

Related Conditions & MeSH terms

• Malaria

Locations

Country	Name	City	State
Mali	Malaria Research and Training Center	Bamako

Sponsors (1)

Lead Sponsor	Collaborator
National Institute of Allergy and Infectious Diseases (NIAID)

Country where clinical trial is conducted

Mali, 

References & Publications (3)

Achidi EA, Perlmann H, Salimonu LS, Perlmann P, Walker O, Asuzu MC. A longitudinal study of seroreactivities to Plasmodium falciparum antigens in Nigerian infants during their first year of life. Acta Trop. 1995 May;59(2):173-83. — View Citation

ALLISON AC. Glucose-6-phosphate dehydrogenase deficiency in red blood cells of East Africans. Nature. 1960 May 14;186:531-2. — View Citation

ALLISON AC. Protection afforded by sickle-cell trait against subtertian malareal infection. Br Med J. 1954 Feb 6;1(4857):290-4. — View Citation