Skip to main content
Log in

Analyses des réponses IgG dirigées contre des antigènes candidats vaccins dans le paludisme urbain non aggravé à Dakar (Sénégal) : variations suivant l’âge et les densités parasitaires

IgG responses to candidate malaria vaccine antigens in the urban area of Dakar (Senegal): evolution according to age and parasitemia in patients with mild symptoms

  • Parasitologie / Parasitology
  • Published:
Bulletin de la Société de pathologie exotique

Résumé

L’évaluation de la spécificité des IgG anti-plasmodium vis-à-vis d’antigènes candidats vaccins a rarement porté sur le paludisme urbain dont les accès cliniques couvrent toutes les classes d’âge et peuvent devenir sévères. Cette étude rétrospective évalue par ELISA les taux d’IgG et de sous-classes d’IgG contre les protéines MSP1p19, MSP3, EB200, GST-5 et R23 de P. falciparum. Elle a été faite chez 200 patients dakarois consultant pour un accès palustre non aggravé. Un âge moyen de 15 ans (4 à 56 ans) et des parasitémies entre 0,1 et 17 % ont été retrouvés. Les taux d’IgG anti-MSP3 sont très élevés chez les patients faiblement parasités (≤ 1 %) et apparaissent négativement corrélés aux densités parasitaires (Rho =.0,54 ; p =0,021). Cette corrélation est plus forte chez les enfants (≤15 ans). Une hausse des IgG anti-MSP1p19 chez les adultes à faibles parasitémies (< 1 %) (p = 0,021) avec prédominance de la sous classe IgG1 (p<0,01) a été aussi retrouvée. Ces résultats montrent l’existence d’une association entre réponses Ac et parasitémies dépendante des IgG anti-MSP3 chez les enfants et des IgG anti-MSP1p19 chez les adultes en milieu urbain.

Abstract

Malaria remains a major problem in African countries despite substantial decreases in morbidity and mortality due to sustained control programs. Studies for the evaluation of qualitative or quantitative Ab responses to key targets of anti-plasmodium immunity were mostly done in rural endemic setting compared to urban area. In a cohort of 200 patients with mild malaria and living in Dakar, we analyze total and subclasses IgG responses to a panel of P. falciparum blood stage antigens: MSP1p19, MSP3, EB200, GST-5 and R23. A mean age of 15 yrs (4 to 56 yrs) and parasitemia between 0.1 to 17% were found. Levels of IgG anti-MSP3 were higher in patients with low parasitemia (≤1 %) and appear negatively correlated to parasite densities (Rho =. 0.54; p= 0.021). This correlation is more significant in children (≤ 15 yrs). In addition, an increase of IgG responses against MSP1p19 is highly observed in adults having a parasitemia less than 1 %. In those patients, we find that IgG1 subclasses were predominant (p <0.01). Our study shows an association between Ab responses and parasitemia. This association is dependant to IgG anti-MSP3 in children and IgG anti-MSP1p19 in adults living in urban area.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Références

  1. Bonnefoy S, Guillotte M, Langsley G, Mercereau-Puijalon O (1992) Plasmodium falciparum: characterization of gene R45 encoding a trophozoite antigen containing a central block of six amino acid repeats. Exp Parasitol 74(4):441–51

    Article  CAS  PubMed  Google Scholar 

  2. Bouharoun-Tayoun H, Attanath P, Sabchareon A, et al (1990) Antibodies that protect humans against Plasmodium falciparum blood stages do not on their own inhibit parasite growth and invasion in vitro, but act in cooperation with monocytes. J Exp Med 172(6):1633–41

    Article  CAS  PubMed  Google Scholar 

  3. Byrne N (2007) Urban malaria risk in sub-Saharan Africa: where is the evidence? Travel Med Infect Dis 5(2):135–7

    Article  PubMed  Google Scholar 

  4. Cohen S, Mac Gregor IA, Carrington SC (1961) Gamma globuline acquired immunity to human malaria. Nature 192:733–7

    Article  CAS  PubMed  Google Scholar 

  5. Courtin D, Oesterholt M, Huismans H, et al (2009) The quantity and quality of African children’s IgG responses to merozoite surface antigens reflect protection against Plasmodium falciparum malaria. PLoS One 4(10):e7590

    Article  Google Scholar 

  6. Dodoo D, Atuguba F, Bosomprah S, et al (2011) Antibody levels to multiple malaria vaccine candidate antigens in relation to clinical malaria episodes in children in the Kasena-Nankana district of Northern Ghana. Malar J 10:108

    Article  PubMed Central  PubMed  Google Scholar 

  7. Dodoo D, Hollingdale MR, Anum D, et al (2011) Measuring naturally acquired immune responses to candidate malaria vaccine antigens in Ghanaian adults. Malar J 10:168

    Article  PubMed Central  PubMed  Google Scholar 

  8. Fowkes FJ, Richards JS, Simpson JA, Beeson JG (2010) The relationship between anti-merozoite antibodies and incidence of Plasmodium falciparum malaria: A systematic review and metaanalysis. PLoS Med 7(1):e1000218

    Article  Google Scholar 

  9. Hay SI, Guerra CA, Tatem AJ, et al (2005) Urbanization, malaria transmission and disease burden in Africa. Nat Rev Microbiol 3(1):81–90

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  10. Iriemenam NC, Khirelsied AH, Nasr A, et al (2009) Antibody responses to a panel of Plasmodium falciparum malaria bloodstage antigens in relation to clinical disease outcome in Sudan. Vaccine 27(1):62–71

    Article  CAS  PubMed  Google Scholar 

  11. Lundquist R, Nielsen LK, Jafarshad A, et al (2006) Human recombinant antibodies against Plasmodium falciparum merozoite surface protein 3 cloned from peripheral blood leukocytes of individuals with immunity to malaria demonstrate antiparasitic properties. Infect Immun 74(6):3222–31

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  12. Mattei D, Scherf A (1992) The Pf332 gene codes for a megadalton protein of Plasmodium falciparum asexual blood stages. Mem Inst Oswaldo Cruz 87 Suppl 3:163–8

    Article  PubMed  Google Scholar 

  13. Mbengue B, Diatta AM, Tall A, et al (2010) Antibodies responses to Plasmodium falciparum blood stage crude extract in symptomatic patients living in an urban, low endemic area of Dakar (Senegal). Dakar Médical 55(3):20–6

    Google Scholar 

  14. Mbengue B, Niang B, Diatta B, et al (2010) The use of crude Plasmodium falciparum antigens for comparison of antibody responses in patients with mild malaria vs. cerebral malaria. Iran J Immunol 7(3):150–61

    CAS  PubMed  Google Scholar 

  15. Nebie I, Diarra A, Ouedraogo A, et al (2008) Humoral responses to Plasmodium falciparum blood-stage antigens and association with incidence of clinical malaria in children living in an area of seasonal malaria transmission in Burkina Faso, West Africa. Infect Immun 76(2):759–66

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  16. Oeuvray C, Bouharoun-Tayoun H, Grass-Masse H, et al (1994) A novel merozoite surface antigen of Plasmodium falciparum (MSP-3) identified by cellular-antibody cooperative mechanism antigenicity and biological activity of antibodies. Mem Inst Osw Cruz 89 2:77–80

    Article  Google Scholar 

  17. Branch OH, Udhayakumar V, Hightower AW, et al (1998) A longitudinal investigation of IgG and IgM antibody responses to the merozoite surface protein-1 19-kiloDalton domain of Plasmodium falciparum in pregnant women and infants: associations with febrile illness, parasitemia, and anemia. Am J Trop Med Hyg, 58(2):211–9

    CAS  PubMed  Google Scholar 

  18. Perraut R, Marrama L, Diouf B, et al (2005) Antibodies to the conserved C-terminal domain of the Plasmodium falciparum merozoite surface protein 1 and to the merozoite extract and their relationship with in vitro inhibitory antibodies and protection against clinical malaria in a Senegalese village. J Infect Dis 191(2):264–71

    Article  CAS  PubMed  Google Scholar 

  19. Perraut R, Morales-Betoulle S, Le Scanf C, et al (2000) Evaluation of immunogenicity and protective efficacy of carrier-free Plasmodium falciparum R23 antigen in pre-exposed saimiri sciureus monkeys. Vaccine 19(1):59–67

    Article  CAS  PubMed  Google Scholar 

  20. Programme National de Lutte contre le paludisme, Partenariat Sénégal, Rapport 2012. Avril 2013. p. 1-56

  21. Robert V, Macintyre K, Keating J, et al (2003) Malaria transmission in urban sub-Saharan Africa. Am J Trop Med Hyg 68(2):169–76

    PubMed  Google Scholar 

  22. Roussilhon C, Oeuvray C, Müller-Graf C, et al (2007) Long-term clinical protection from falciparum malaria is strongly associated with IgG3 antibodies to merozoite surface protein 3. PLoS Med 4(11):e320

    Article  Google Scholar 

  23. Sergent E (1950) Définition de l’immunité et de la prémunition. Arch Inst Pasteur Alger 28(4):429–40

    CAS  PubMed  Google Scholar 

  24. Stanisic DI, Richards JS, McCallum FJ, et al (2009) Immunoglobulin G subclass-specific responses against Plasmodium falciparum merozoite antigens are associated with control of parasitemia and protection from symptomatic illness. Infect Immun 77(3):1165–74

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  25. Trape JF, Rogier C, Konate L, et al (1994) The Dielmo project: a longitudinal study of natural malaria infection and the mechanisms of protective immunity in a community living in a holoendemic area of Senegal. Am J Trop Med Hyg 51(2):123–37

    CAS  PubMed  Google Scholar 

  26. Trape JF, Zoulani A (1987) Malaria and urbanization in central Africa: the example of Brazzaville. Part III: Relationships between urbanization and the intensity of malaria transmission. Trans R Soc Trop Med Hyg 81(Suppl 2):19–25

    Article  PubMed  Google Scholar 

  27. WHO Geneva (2000) Severe falciparum malaria. World Health Organization, Communicable Diseases Cluster. Trans R Soc Trop Med Hyg 94(Suppl 1):S1–90

    Article  Google Scholar 

  28. WHO Geneva (2014) World malaria report 2013, 255 p

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to B. Mbengue.

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mbengue, B., Sylla Niang, M., Ndiaye Diallo, R. et al. Analyses des réponses IgG dirigées contre des antigènes candidats vaccins dans le paludisme urbain non aggravé à Dakar (Sénégal) : variations suivant l’âge et les densités parasitaires. Bull. Soc. Pathol. Exot. 108, 94–101 (2015). https://doi.org/10.1007/s13149-015-0419-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13149-015-0419-4

Mots clés

Keywords

Navigation