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Maternal CD4+ microchimerism in HIV-exposed newborns after spontaneous vaginal delivery or caesarean section.
Buxmann, H; Reitter, A; Bapistella, S; Stürmer, M; Königs, C; Ackermann, H; Louwen, F; Bader, P; Schlößer, R L; Willasch, A M.
Affiliation
  • Buxmann H; Goethe University, Department for Children and Adolescents, Division for Neonatology, University Hospital Frankfurt/Main, Germany. Electronic address: horst.buxmann@kgu.de.
  • Reitter A; Department of Gynecology and Obstetrics, Division of Obstetrics and Prenatal Medicine, University Hospital Frankfurt/Main, Germany.
  • Bapistella S; Goethe University, Department for Children and Adolescents, Division for Neonatology, University Hospital Frankfurt/Main, Germany.
  • Stürmer M; Institute for Medical Virology, University Hospital Frankfurt/Main, Germany.
  • Königs C; Department for Children and Adolescents, Division for Stem Cell Transplantation and Immunology, University Hospital Frankfurt/Main, Germany.
  • Ackermann H; Institute of Biostatistics and Mathematical Modeling, University Hospital Frankfurt/Main, Germany.
  • Louwen F; Department of Gynecology and Obstetrics, Division of Obstetrics and Prenatal Medicine, University Hospital Frankfurt/Main, Germany.
  • Bader P; Department for Children and Adolescents, Division for Stem Cell Transplantation and Immunology, University Hospital Frankfurt/Main, Germany.
  • Schlößer RL; Goethe University, Department for Children and Adolescents, Division for Neonatology, University Hospital Frankfurt/Main, Germany.
  • Willasch AM; Department for Children and Adolescents, Division for Stem Cell Transplantation and Immunology, University Hospital Frankfurt/Main, Germany.
Early Hum Dev ; 98: 49-55, 2016 07.
Article in En | MEDLINE | ID: mdl-27351353
ABSTRACT

BACKGROUND:

Maternal CD4+ cell microchimerism may be greater after caesarean section compared to spontaneous vaginal delivery and could cause mother-to-child transmission (MTCT) in HIV-exposed newborns.

AIMS:

To evaluate maternal CD4+ cell microchimerism in HIV-exposed newborns after spontaneous vaginal delivery or caesarean section. STUDY DESIGN AND

SUBJECTS:

In this prospective single-centre study, neonates whose mothers were infected with HIV and had normal MTCT risk according to the German Austrian Guidelines were considered for study enrolment. Maternal CD4+ cell microchimerism in the newborns' umbilical cord blood was measured and compared by mode of delivery.

RESULTS:

Thirty-seven HIV-infected mothers and their 39 newborns were included in the study. None of the 17 (0.0%) newborns delivered vaginally had quantifiable maternal CD4+ cells (95% confidence interval (CI) 0.00-0.00) in their circulation at birth compared with four of 16 (25.0%) newborns delivered via planned caesarean section, who showed 0.01-0.66% maternal cells (95% CI -0.06-0.16; P=0.02) in their circulation. The intention to treat analysis, which included six additional newborns delivered by unplanned caesarean section, showed quantifiable maternal CD4+ cells in one (0.05%; 95% CI -0.02-0.04) of 23 (4.3%) newborn at birth compared to four of 16 (25.0%) born via planned caesarean section (95% CI -0.06-0.16; P=0.04). There was no MTCT in any of the newborns.

CONCLUSION:

In this small cohort, spontaneous vaginal delivery in HIV-infected women with normal MTCT risk was associated with lower maternal CD4+ cell transfer to newborns compared to planned caesarean section.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Health context: 2_ODS3 Database: MEDLINE Main subject: Pregnancy Complications, Infectious / CD4-Positive T-Lymphocytes / HIV Infections / Cesarean Section / Infectious Disease Transmission, Vertical Type of study: Clinical_trials Limits: Adult / Female / Humans / Male / Newborn / Pregnancy Language: En Journal: Early Hum Dev Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 2_ODS3 Database: MEDLINE Main subject: Pregnancy Complications, Infectious / CD4-Positive T-Lymphocytes / HIV Infections / Cesarean Section / Infectious Disease Transmission, Vertical Type of study: Clinical_trials Limits: Adult / Female / Humans / Male / Newborn / Pregnancy Language: En Journal: Early Hum Dev Year: 2016 Document type: Article