Abstract
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Infection and Immunity |
| Vol/bind | 73 |
| Udgave nummer | 7 |
| Sider (fra-til) | 4112-8 |
| Antal sider | 6 |
| ISSN | 0019-9567 |
| DOI | |
| Status | Udgivet - 2005 |
Bibliografisk note
Keywords: Adolescent; Adult; Antibodies, Protozoan; Antigens, Protozoan; Disease Transmission, Vertical; Female; Humans; Immunoglobulin G; Malaria, Falciparum; Middle Aged; Multivariate Analysis; Parity; Pregnancy; Pregnancy Complications, ParasiticAdgang til dokumentet
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I: Infection and Immunity, Bind 73, Nr. 7, 2005, s. 4112-8.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
}
TY - JOUR
T1 - Effects of pregnancy and intensity of Plasmodium falciparum transmission on immunoglobulin G subclass responses to variant surface antigens
AU - Megnekou, Rosette
AU - Staalsoe, Trine
AU - Taylor, Diane W
AU - Leke, Rose
AU - Hviid, Lars
N1 - Keywords: Adolescent; Adult; Antibodies, Protozoan; Antigens, Protozoan; Disease Transmission, Vertical; Female; Humans; Immunoglobulin G; Malaria, Falciparum; Middle Aged; Multivariate Analysis; Parity; Pregnancy; Pregnancy Complications, Parasitic
PY - 2005
Y1 - 2005
N2 - Placenta-sequestering Plasmodium falciparum involved in the pathogenesis of pregnancy-associated malaria (PAM) in otherwise clinically immune women expresses particular variant surface antigens (VSA(PAM)) on the surface of infected erythrocytes that differ from VSA found in parasitized nonpregnant individuals (non-PAM type VSA). We studied levels of immunoglobulin G (IgG) and IgG subclasses with specificity for VSA(PAM) and for non-PAM type VSA in pregnant and nonpregnant women from two sites with different endemicities in Cameroon. We found that VSA(PAM)-specific responses depended on the pregnancy status, parity, gestational age, and parasite transmission intensity, whereas only the parasite transmission intensity influenced the levels of IgG specific for non-PAM type VSA. For both types of VSA, the responses were dominated by the cytophilic subclass IgG1, followed by IgG3. In pregnant women, the levels of VSA(PAM)-specific antibodies either were very low or negative or were very high, whereas the levels of the antibodies specific for non-PAM type VSA were uniformly high. Interestingly, the levels of VSA(PAM)-specific IgG1 increased with increasing gestational age, while the levels of the corresponding IgG3 tended to decrease with increasing gestational age. The IgG subclass responses with specificity for non-PAM type VSA did not vary significantly with gestational age. Taken together, our data indicate that IgG1 and to a lesser extent IgG3 are the main subclasses involved in acquired VSA(PAM)-specific immunity to pregnancy-associated malaria.
AB - Placenta-sequestering Plasmodium falciparum involved in the pathogenesis of pregnancy-associated malaria (PAM) in otherwise clinically immune women expresses particular variant surface antigens (VSA(PAM)) on the surface of infected erythrocytes that differ from VSA found in parasitized nonpregnant individuals (non-PAM type VSA). We studied levels of immunoglobulin G (IgG) and IgG subclasses with specificity for VSA(PAM) and for non-PAM type VSA in pregnant and nonpregnant women from two sites with different endemicities in Cameroon. We found that VSA(PAM)-specific responses depended on the pregnancy status, parity, gestational age, and parasite transmission intensity, whereas only the parasite transmission intensity influenced the levels of IgG specific for non-PAM type VSA. For both types of VSA, the responses were dominated by the cytophilic subclass IgG1, followed by IgG3. In pregnant women, the levels of VSA(PAM)-specific antibodies either were very low or negative or were very high, whereas the levels of the antibodies specific for non-PAM type VSA were uniformly high. Interestingly, the levels of VSA(PAM)-specific IgG1 increased with increasing gestational age, while the levels of the corresponding IgG3 tended to decrease with increasing gestational age. The IgG subclass responses with specificity for non-PAM type VSA did not vary significantly with gestational age. Taken together, our data indicate that IgG1 and to a lesser extent IgG3 are the main subclasses involved in acquired VSA(PAM)-specific immunity to pregnancy-associated malaria.
U2 - 10.1128/IAI.73.7.4112-4118.2005
DO - 10.1128/IAI.73.7.4112-4118.2005
M3 - Journal article
C2 - 15972500
SN - 0019-9567
VL - 73
SP - 4112
EP - 4118
JO - Infection and Immunity
JF - Infection and Immunity
IS - 7
ER -