Literature DB >> 9574782

Seasonal variation in agglutination of Plasmodium falciparum-infected erythrocytes.

H A Giha1, T G Theander, T Staalsø, C Roper, I M Elhassan, H Babiker, G M Satti, D E Arnot, L Hviid.   

Abstract

Agglutination and rosette formation are in vitro characteristics of Plasmodium falciparum-infected erythrocytes, which have been associated with host protective immune responses and also with parasite virulence. The present study was carried out in an area of seasonal and unstable malaria transmission in eastern Sudan. Plasma samples were obtained before, during, and after the transmission season from a volunteer cohort of 64 individuals seven years of age and older. These plasmas were assayed for their ability to agglutinate cultured parasitized erythrocytes originally obtained from acute malaria infection samples taken from five of the cohort members. Our data show that the capacity of donor plasma samples to agglutinate parasitized cells depended largely on the time of sampling relative to the transmission season, at least within this epidemiologic setting. Thus, although less than half of the pretransmission season samples could agglutinate any of the five lines of cultured parasites, all post-transmission season samples could agglutinate at least one of the parasite lines, with 74% agglutinating two or more lines. This increase in the agglutination capacity of individual plasma samples after the transmission season occurred essentially regardless of whether an individual had experienced a clinical malaria attack during the transmission season. The study thus confirms the acquisition of agglutinating antibodies following episodes of clinical malaria, but also demonstrates that such acquisition can take place in the absence of disease, presumably as a consequence of subclinical infection. This is the first demonstration of marked seasonal fluctuations in the capacity of individuals' sera to agglutinate parasitized red blood cells. Possible explanations for this effect include a decrease in the levels of agglutinating antibodies between seasons, or shifts in the antigens being recognized by such antibodies from one transmission season to the next. Finally, we showed the existence of marked seasonal fluctuation in the levels of agglutinating antibodies, either because levels of such antibodies are not sustained between seasons or because the antigens recognized change from one season to the next.

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Year:  1998        PMID: 9574782     DOI: 10.4269/ajtmh.1998.58.399

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  16 in total

1.  Differential patterns of human immunoglobulin G subclass responses to distinct regions of a single protein, the merozoite surface protein 1 of Plasmodium falciparum.

Authors:  D R Cavanagh; C Dobaño; I M Elhassan; K Marsh; A Elhassan; L Hviid; E A Khalil; T G Theander; D E Arnot; J S McBride
Journal:  Infect Immun       Date:  2001-02       Impact factor: 3.441

2.  The surface variant antigens of Plasmodium falciparum contain cross-reactive epitopes.

Authors:  B Gamain; L H Miller; D I Baruch
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-13       Impact factor: 11.205

3.  Characterization of the antibody response against Plasmodium falciparum erythrocyte membrane protein 1 in human volunteers.

Authors:  Darren R Krause; Michelle L Gatton; Sarah Frankland; Damon P Eisen; Michael F Good; Leann Tilley; Qin Cheng
Journal:  Infect Immun       Date:  2007-10-08       Impact factor: 3.441

Review 4.  Virulence in malaria: an evolutionary viewpoint.

Authors:  Margaret J Mackinnon; Andrew F Read
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2004-06-29       Impact factor: 6.237

5.  Differences in human antibody reactivity to Plasmodium falciparum variant surface antigens are dependent on age and malaria transmission intensity in northeastern Tanzania.

Authors:  Lasse S Vestergaard; John P Lusingu; Morten A Nielsen; Bruno P Mmbando; Daniel Dodoo; Bartholomew D Akanmori; Michael Alifrangis; Ib C Bygbjerg; Martha M Lemnge; Trine Staalsoe; Lars Hviid; Thor G Theander
Journal:  Infect Immun       Date:  2008-02-04       Impact factor: 3.441

6.  Exposure to Diverse Plasmodium falciparum Genotypes Shapes the Risk of Symptomatic Malaria in Incident and Persistent Infections: A Longitudinal Molecular Epidemiologic Study in Kenya.

Authors:  Kelsey M Sumner; Elizabeth Freedman; Judith N Mangeni; Andrew A Obala; Lucy Abel; Jessie K Edwards; Michael Emch; Steven R Meshnick; Brian W Pence; Wendy Prudhomme-O'Meara; Steve M Taylor
Journal:  Clin Infect Dis       Date:  2021-10-05       Impact factor: 9.079

Review 7.  The complexities of malaria disease manifestations with a focus on asymptomatic malaria.

Authors:  Dolie D Laishram; Patrick L Sutton; Nutan Nanda; Vijay L Sharma; Ranbir C Sobti; Jane M Carlton; Hema Joshi
Journal:  Malar J       Date:  2012-01-31       Impact factor: 2.979

8.  FcgammaRIIa (CD32) polymorphism and anti-malarial IgG subclass pattern among Fulani and sympatric ethnic groups living in eastern Sudan.

Authors:  Amre Nasr; Nnaemeka C Iriemenam; Hayder A Giha; Halima A Balogun; Robin F Anders; Marita Troye-Blomberg; Gehad ElGhazali; Klavs Berzins
Journal:  Malar J       Date:  2009-03-13       Impact factor: 2.979

Review 9.  What you see is not what you get: implications of the brevity of antibody responses to malaria antigens and transmission heterogeneity in longitudinal studies of malaria immunity.

Authors:  Samson M Kinyanjui; Philip Bejon; Faith H Osier; Peter C Bull; Kevin Marsh
Journal:  Malar J       Date:  2009-10-28       Impact factor: 2.979

10.  Antibody recognition of Plasmodium falciparum erythrocyte surface antigens in Kenya: evidence for rare and prevalent variants.

Authors:  P C Bull; B S Lowe; M Kortok; K Marsh
Journal:  Infect Immun       Date:  1999-02       Impact factor: 3.441

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