Lymphocyte subpopulations in malaria infected individuals living in an endemic area

Southeast Asian Journal of Tropical Medicine and Public Health

Volumn 34, Issue 2, 2003, Pages 310-315

  Srisurapanon, Surangrat ^a   Wiwattanakul, S ^a   Apibal, S ^b   Suwannuruk, R ^b   Sujimanaskul, S ^c   Petchsuwan, B ^c   Pattanapanyasat, K ^d  

^a SRINAKHARINWIROT UNIVERSITY   (Thailand)

^b MAHIDOL UNIVERSITY   (Thailand)

^c NAVAMINDRADHIRAJ UNIVERSITY   (Thailand)

^d MAHIDOL UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIMALARIAL AGENT; CD8 ANTIGEN;

ADOLESCENT; ADULT; ARTICLE; CELL ACTIVITY; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOTOXIC LYMPHOCYTE; DEVICE; ENDEMIC DISEASE; FLOW CYTOMETRY; HUMAN; HUMAN CELL; LYMPHOCYTE COUNT; LYMPHOCYTE SUBPOPULATION; MALARIA; PLASMODIUM VIVAX; STATISTICAL SIGNIFICANCE; STIMULATION; TH2 CELL;

EID: 0141852375     PISSN: 01251562     EISSN: 26975718     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

1. Autran B, Legac E, Blanc C, Debre P. A Th0/Th2-like function of CD4+CD7-T helper cells from normal donors and HIV-infected patients. J Immunol 1995; 154: 1408-17.
2. De Souza JB, Williamson KH, Otani T, Playfair JH. Early gamma interferon responses in lethal and nonlethal murine blood-stage malaria. Infect Immun 1997; 65: 1593-8.
3. Del Prete G, Maggi E, Romagnani S. Human Th1 and Th2 cells: functional properties, mechanisms of regulation, and role in disease. Lab Invest 1994; 70: 299-306.
4. Elhassan IM, Hviid L, Satti G, et al. Evidence of endothelial inflammation, T cell activation, and T cell reallocation in uncomplicated Plasmodium falciparum malaria. Am J Trop Med Hyg 1994; 51: 372-9.
5. Ferrante P, Fusi ML, Saresella M, et al. Cytokine production and surface marker expression in acute and stable multiple sclerosis: altered IL-12 production and augmented signaling lymphocytic activation molecule (SLAM)-expressing lymphocytes in acute multiple sclerosis. J Immunol 1998; 160: 1514-21.
6. Hirunpetcharat C, Finkelman F, Clark IA, Good MF. Malaria parasite-specific Th1-like T cells simultaneously reduce parasitemia and promote disease. Parasite Immunol 1999; 21: 319-29.
7. Hviid L, Kemp K, Kern P, et al. What is the cause of lymphopenia in malaria? Infect Immun 2000; 68: 6087-9.
8. Hviid L, Kurtzhals JA, Goka BQ, Oliver-Commey, JO, Nkrumah FK, Theander TG. Rapid reemergence of T cells into peripheral circulation following treatment of severe and uncomplicated Plasmodium falciparum malaria. Infect Immun 1997; 65: 4090-3.
9. Jason J, Archibald LK, Nwanyanwu OC, et al. Cytokines and malaria parasitemia. Clin Immunol 2001; 100: 208-18.
10. Kemp K, Akanmori BD, Adabayeri V, et al. Cytokine production and apoptosis among T cells from patients under treatment for Plasmodium falciparum malaria. Clin Exp Immunol 2002; 127: 151-7.
11. Kern P, Dietrich M, Hemmer C, Wellinghausen N. Increased levels of soluble Fas ligand in serum in Plasmodium falciparum malaria. Infect Immun 2000; 68: 3061-3.
12. Langhorne J, Cross C, Seixas E, Li C, von der Weid T. A role for B cells in the development of T cell helper function in a malaria infection in mice. Proc Natl Acad Sci USA 1998; 95: 1730-4.
13. Leblond B, Othman TB, Blanc C, et al. Expansion of CD4+CD7-T cells, a memory subset with preferential interleukin-4 production, after bone marrow transplantation. Transplantation 1997; 64: 1453-9.
14. Legac E, Autran B, Merle-Beral H, Katlama C, Debre P. CD4+CD7-CD57+T cells: a new T-lymphocyte subset expanded during human immunodeficiency virus infection. Blood 1992; 79: 1746-53.
15. Lucey DR, Clerici M, Shearer GM. Type 1 and type 2 Cytokine dysregulation in human infectious, neoplastic, and inflammatory diseases. Clin Microbiol Rev 1996; 9: 532-62.
16. Matsumoto J, Kawai S, Terao K, et al. Malaria infection induces rapid elevation of the soluble Fas ligand level in serum and subsequent T lymphocytopenia: possible factors responsible for the differences in susceptibility of two species of Macaca monkeys to Plasmodium coatneyi infection. Infect Immun 2000; 68: 1183-8.
17. Reece WHH, Plebanski M, Akinwunmi P, et al. Naturally exposed populations differ in their T1 and T2 responses to the circumsporozoite protein of Plasmodium falciparum. Infect. Immun 2002; 70: 1468-1474.
18. Reinhold U, Liu L, Sesterhenn J, Schnautz S, Abken H. The CD7-T cell subset represents the majority of IL-5-secreting cells within CD4+ CD45RA-T cells. Clin Exp Immunol 1996; 106: 555-9.
19. Riley EM, Rowe P, Allen SJ, Greenwood BM. Soluble plasma IL-2 receptors and malaria. Clin Exp Immunol 1993; 91: 495-9.
20. Stevenson MM, Tam MF. Differential induction of helper T cell subsets during blood-stage Plasmodium chabaudi AS infection in resistant and susceptible mice. Clin Exp Immunol 1993; 92: 77-83.
21. Taylor-Robinson AW, Phillips RS, Severn A, Moncada S, Liew FY. The role of TH1 and TH2 cells in a rodent malaria infection. Science 1993; 260: 931-4.
22. Tongtawe P, Chaicumpa W, Tapchaisri P, Looareesuwan S, Webster HK. Lymphocyte subpopulations during acute and convalescence phases of malaria. Asian Pac J Allergy Immunol 1988; 6: 11-8.
23. Torre D, Speranza F, Giola M, Matteelli A, Tambini R, Biondi G. Role of Th1 and Th2 cytokines in immune response to uncomplicated Plasmodium falciparum malaria. Clin Diagn Lab Immunol 2002; 9: 348-351.
24. Winkler S, Willheim M, Baier K, et al. Reciprocal regulation of Th1- and Th2-cytokine-producing T cells during clearance of parasitemia in Plasmodium falciparum malaria. Infect Immun 1998; 66: 6040-4.
25. Yoshimoto T, Paul WE. CD4pos, NK1.1pos T cells promptly produce interleukin 4 in response to in vivo challenge with anti-CD3. J Exp Med 1994; 179: 1285-95.