Relationships between maternal malaria and malarial immune responses in mothers and neonates

F N Rasheed; J N Bulmer; A De Francisco; M F Jawla; P H Jakobsen; A Jepson; B M Greenwood

Relationships between maternal malaria and malarial immune responses in mothers and neonates

F N Rasheed, J N Bulmer, A De Francisco, M F Jawla, P H Jakobsen, A Jepson, B M Greenwood

Centre for Medical Parasitology

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

62 Citationer (Scopus)

Abstract

Udgivelsesdato: 1995-Jan

Originalsprog	Engelsk
Tidsskrift	Parasite Immunology
Vol/bind	17
Udgave nummer	1
Sider (fra-til)	1-10
Antal sider	9
ISSN	0141-9838
Status	Udgivet - 1995

Bibliografisk note

Keywords: Adolescent; Adult; Animals; Antibodies, Protozoan; Case-Control Studies; Female; Fetal Blood; Humans; Hydrocortisone; Immunity, Maternally-Acquired; Immunoglobulin G; Immunoglobulin M; Infant, Newborn; Malaria, Falciparum; Plasmodium falciparum; Pregnancy; Pregnancy Complications, Parasitic

Citationsformater

@article{8c5236d01d5811df8ed1000ea68e967b,

title = "Relationships between maternal malaria and malarial immune responses in mothers and neonates",

abstract = "Immune responses of 97 Gambian women and their neonates were studied. New methods distinguished between active and previous placental malaria, were used to examine relationships between maternal malaria and neonatal immune responses. Many placentas (61%) had active or previous malarial infection. Maternal and cord malarial IgG levels correlated (P < 0.001). Malarial IgG was raised in cord blood in active placental malaria; IgM was not detected. Mean lymphoproliferation and the proportion of responders to soluble P. falciparum antigens (F32) and conserved regions of p190 expressed on trophozoites and schizonts (190L and 190N) were higher in neonates than mothers. There was no clear relationship between maternal malaria and neonatal mean lymphoproliferation to malarial antigens, although fewer neonates responded when mothers were actively infected. Matched maternal and neonatal lymphoproliferation responses did not correlate. However, first born neonatal lymphoproliferation to PPD and malarial antigens appeared lower than other neonates, in agreement with lower lymphoproliferation in primigravidae compared with multigravidae. Also in common with mothers, autologous plasma suppressed neonatal lymphoproliferation to PPD and malarial antigens, suggesting common immunoregulation. Higher cortisol or other circulating factors in first pregnancies may be implicated. The relevance of cell-mediated malarial immune responses detected at birth remains to be established.",

author = "Rasheed, {F N} and Bulmer, {J N} and {De Francisco}, A and Jawla, {M F} and Jakobsen, {P H} and A Jepson and Greenwood, {B M}",

note = "Keywords: Adolescent; Adult; Animals; Antibodies, Protozoan; Case-Control Studies; Female; Fetal Blood; Humans; Hydrocortisone; Immunity, Maternally-Acquired; Immunoglobulin G; Immunoglobulin M; Infant, Newborn; Malaria, Falciparum; Plasmodium falciparum; Pregnancy; Pregnancy Complications, Parasitic",

year = "1995",

language = "English",

volume = "17",

pages = "1--10",

journal = "Parasite Immunology",

issn = "0141-9838",

publisher = "Wiley-Blackwell",

number = "1",

}

TY - JOUR

T1 - Relationships between maternal malaria and malarial immune responses in mothers and neonates

AU - Rasheed, F N

AU - Bulmer, J N

AU - De Francisco, A

AU - Jawla, M F

AU - Jakobsen, P H

AU - Jepson, A

AU - Greenwood, B M

N1 - Keywords: Adolescent; Adult; Animals; Antibodies, Protozoan; Case-Control Studies; Female; Fetal Blood; Humans; Hydrocortisone; Immunity, Maternally-Acquired; Immunoglobulin G; Immunoglobulin M; Infant, Newborn; Malaria, Falciparum; Plasmodium falciparum; Pregnancy; Pregnancy Complications, Parasitic

PY - 1995

Y1 - 1995

N2 - Immune responses of 97 Gambian women and their neonates were studied. New methods distinguished between active and previous placental malaria, were used to examine relationships between maternal malaria and neonatal immune responses. Many placentas (61%) had active or previous malarial infection. Maternal and cord malarial IgG levels correlated (P < 0.001). Malarial IgG was raised in cord blood in active placental malaria; IgM was not detected. Mean lymphoproliferation and the proportion of responders to soluble P. falciparum antigens (F32) and conserved regions of p190 expressed on trophozoites and schizonts (190L and 190N) were higher in neonates than mothers. There was no clear relationship between maternal malaria and neonatal mean lymphoproliferation to malarial antigens, although fewer neonates responded when mothers were actively infected. Matched maternal and neonatal lymphoproliferation responses did not correlate. However, first born neonatal lymphoproliferation to PPD and malarial antigens appeared lower than other neonates, in agreement with lower lymphoproliferation in primigravidae compared with multigravidae. Also in common with mothers, autologous plasma suppressed neonatal lymphoproliferation to PPD and malarial antigens, suggesting common immunoregulation. Higher cortisol or other circulating factors in first pregnancies may be implicated. The relevance of cell-mediated malarial immune responses detected at birth remains to be established.

AB - Immune responses of 97 Gambian women and their neonates were studied. New methods distinguished between active and previous placental malaria, were used to examine relationships between maternal malaria and neonatal immune responses. Many placentas (61%) had active or previous malarial infection. Maternal and cord malarial IgG levels correlated (P < 0.001). Malarial IgG was raised in cord blood in active placental malaria; IgM was not detected. Mean lymphoproliferation and the proportion of responders to soluble P. falciparum antigens (F32) and conserved regions of p190 expressed on trophozoites and schizonts (190L and 190N) were higher in neonates than mothers. There was no clear relationship between maternal malaria and neonatal mean lymphoproliferation to malarial antigens, although fewer neonates responded when mothers were actively infected. Matched maternal and neonatal lymphoproliferation responses did not correlate. However, first born neonatal lymphoproliferation to PPD and malarial antigens appeared lower than other neonates, in agreement with lower lymphoproliferation in primigravidae compared with multigravidae. Also in common with mothers, autologous plasma suppressed neonatal lymphoproliferation to PPD and malarial antigens, suggesting common immunoregulation. Higher cortisol or other circulating factors in first pregnancies may be implicated. The relevance of cell-mediated malarial immune responses detected at birth remains to be established.

M3 - Journal article

C2 - 7731730

SN - 0141-9838

VL - 17

SP - 1

EP - 10

JO - Parasite Immunology

JF - Parasite Immunology

IS - 1

ER -