Evaluation of the antibody response to Anopheles salivary antigens as a potential marker of risk of malaria

Transactions of the Royal Society of Tropical Medicine and Hygiene

Volumn 100, Issue 4, 2006, Pages 363-370

  Remoue, Franck ^a   Cisse, Badara ^a,b   Ba, Fatou ^a   Sokhna, Cheikh ^a   Herve, Jean Pierre ^c   Boulanger, Denis ^a   Simondon, François ^a  

^a Centre IRD de Hann   (Senegal)

^b LONDON SCHOOL OF HYGIENE AND TROPICAL MEDICINE   (United Kingdom)

^c INSTITUT DE RECHERCHE POUR LE DÉVELOPPEMENT   (France)

Author keywords

Anopheles; Exposure; Immunoepidemiology; Malaria; Senegal; Transmission

Indexed keywords

ANTIMALARIAL AGENT; IMMUNOGLOBULIN G ANTIBODY; PARASITE ANTIGEN; PROTOZOON ANTIBODY;

ANOPHELES GAMBIAE; ANTIBODY RESPONSE; ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DISEASE MARKER; DISEASE TRANSMISSION; EXPOSURE; HUMAN; INFECTION RISK; MAJOR CLINICAL STUDY; MALARIA; METHODOLOGY; NONHUMAN; PLASMODIUM FALCIPARUM; PRESCHOOL CHILD; SALIVA; SEASONAL VARIATION; SENEGAL; STATISTICAL SIGNIFICANCE; ZOOLOGY;

ANIMALS; ANOPHELES GAMBIAE; ANTIGENS, PROTOZOAN; BIOLOGICAL MARKERS; CHILD; CHILD, PRESCHOOL; HUMANS; IMMUNOGLOBULIN G; INFANT; INSECT VECTORS; MALARIA, FALCIPARUM; RISK FACTORS; SALIVA; SEASONS; SENEGAL;

ANOPHELES GAMBIAE; ARTHROPODA; PLASMODIUM FALCIPARUM; PROTOZOA;

EID: 31744436449     PISSN: 00359203     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.trstmh.2005.06.032     Document Type: Article

References (22)

1. A. Barral E. Honda A. Caldas J. Costa V. Vinhas E.D. Rowton J.G. Valenzuela R. Charlab M. Barral-Netto J.M. Ribeiro Human immune response to sand fly salivary gland antigens: A useful epidemiological marker? Am. J. Trop. Med. Hyg. 62 2000 740-745
2. J.G. Breman M.S. Alilio A. Mills Conquering the intolerable burden of malaria: What's new, Ahat's needed: a summary Am. J. Trop. Med. Hyg. 71 2004 1-15
3. H. Brummer-Korvenkontio T. Palosuo G. Francois T. Reunala Characterization of Aedes communis, Aedes aegypti and Anopheles stephensi mosquito saliva antigens by immunoblotting Int. Arch. Allergy Appl. Immunol. 112 1997 169-174
4. R.M. Gordon W. Crewe The mechanisms by which mosquitoes and tsetse-flies obtain their blood-meal, the histology of the lesions produced, and the subsequent reactions of the mammalian host; together with some observations on the feeding of Chrysops and Cimex Ann. Trop. Med. Hyg. 42 1948 334-356
5. R.A. Holt G.M. Subramanian A. Halpern et al. The genome sequence of the malaria mosquito Anopheles gambiae Science 298 2002 129-149
6. A. James P. Rossignol Mosquito salivary glands: Parasitological and molecular aspects Parasitol. Today 7 1991 267-271
7. E.M. Mathenge G.O. Omweri L. Irungu P.N. Ndegwa E. Walczak T.A. Smith G.F. Killeen B.G. Knols Comparative field evaluation of the MBITA trap, the Centers for Disease Control light trap, and the human landing catch for sampling of malaria vectors in western Kenya Am. J. Trop. Med. Hyg. 70 2004 33-37
8. H. Matsuoka H. Matsubara P. Waidhet T. Hashimoto A. Ishii Y. Sato K. Ando Y. Chinzei Depletion of salivary gland proteins in Anopheles stephensi (Diptera: Culicidae) on blood feeding, and induction of antibodies to the proteins in mice being fed Med. Entomol. Zool. 48 1997 211-218
9. R. Nascimento J. Santana S. Lozzi C.N. Araujo A.R. Teixeira Human IgG1 and IgG4: The main antibodies against Triatoma infestans (Hemiptera: Reduviidae) salivary gland proteins Am. J. Trop. Med. Hyg. 65 2001 219-226
10. M. Owhashi M. Harada S. Suguri H. Ohmae A. Ishii The role of saliva of Anopheles stephensi in inflammatory response: Identification of a high molecular weight neutrophil chemotactic factor Parasitol. Res. 87 2001 376-382
11. K. Palosuo H. Brummer-Korvenkontio J. Mikkola T. Sahi T. Reunala Seasonal increase in human IgE and IgG4 antisaliva antibodies to Aedes mosquito bites Int. Arch. Allergy Immunol. 114 1997 367-372
12. R. Ramasamy K. Nagendran M.S. Ramasamy Antibodies to epitopes on merozoite and sporozoite surface antigens as serologic markers of malaria transmission: Studies at a site in the dry zone of Sri Lanka Am. J. Trop. Med. Hyg. 50 1994 537-547
13. J.M. Ribeiro Blood-feeding arthropods: Live syringes or invertebrate pharmacologists? Infect. Agents Dis. 4 1995 143-152
14. V. Robert H. Dieng L. Lochouarn S.F. Traore J.F. Trape F. Simondon D. Fontenille [Malaria transmission in the rural zone of Niakhar, Sénégal] Trop. Med. Int. Health 3 1998 667-677
15. F. Rodhain C. Perez Précis d'entomologie médicale et vétérinaire: Notions d'épidémiologie des maladies à vecteurs 1985 Maloine Paris, France
16. P.A. Rossignol J.M. Ribeiro A. Spielman Increased intradermal probing time in sporozoite-infected mosquitoes Am. J. Trop. Med. Hyg. 33 1984 17-20
17. C. Sadanandane P. Jambulingam S. Subramanian Role of modified CDC miniature light-traps as an alternative method for sampling adult anophelines (Diptera: Culicidae) in the National Mosquitoes Surveillance Programme in India Bull. Entomol. Res. 94 2004 55-63
18. R. Sandeman Immune responses to mosquitoes and flies S.K. Wikel The Immunology of Host-Ectoparasitic Arthropod Relationships 1996 CAB International Wallingford 175-203
19. G. Schoeler S. Wikel Modulation of host immunity by haematophagous arthropods Ann. Trop. Med. Parasitol. 95 2001 755-771
20. B. Schwartz J. Ribeiro M. Goldstein Anti-tick antibodies: An epidemiologic tool in Lyme disease research Am. J. Epidemiol. 132 1990 58-66
21. W. Sykes Negro immunity from malaria and yellow fever BMJ 31 1904 1776-1777
22. H.K. Webster J.B. Gingrich C. Wongsrichanalai S. Tulyayon A. Suvarnamani P. Sookto B. Permpanich Circumsporozoite antibody as a serologic marker of Plasmodium falciparum transmission Am. J. Trop. Med. Hyg. 47 1992 489-497