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Pregnancy-specific responses to COVID-19 revealed by high-throughput proteomics of human plasma.
Gomez-Lopez, Nardhy; Romero, Roberto; Escobar, María Fernanda; Carvajal, Javier Andres; Echavarria, Maria Paula; Albornoz, Ludwig L; Nasner, Daniela; Miller, Derek; Gallo, Dahiana M; Galaz, Jose; Arenas-Hernandez, Marcia; Bhatti, Gaurav; Done, Bogdan; Zambrano, Maria Andrea; Ramos, Isabella; Fernandez, Paula Andrea; Posada, Leandro; Chaiworapongsa, Tinnakorn; Jung, Eunjung; Garcia-Flores, Valeria; Suksai, Manaphat; Gotsch, Francesca; Bosco, Mariachiara; Than, Nandor Gabor; Tarca, Adi L.
Afiliación
  • Gomez-Lopez N; Pregnancy Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services (NICHD/NIH/DHHS), Detroit, MI,
  • Romero R; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA. ngomezlo@med.wayne.edu.
  • Escobar MF; Department of Biochemistry, Microbiology and Immunology, Wayne State University School of Medicine, Detroit, MI, USA. ngomezlo@med.wayne.edu.
  • Carvajal JA; Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI, USA. ngomezlo@med.wayne.edu.
  • Echavarria MP; Pregnancy Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services (NICHD/NIH/DHHS), Detroit, MI,
  • Albornoz LL; Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI, USA. romeror@mail.nih.gov.
  • Nasner D; Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI, USA. romeror@mail.nih.gov.
  • Miller D; Department of Epidemiology and Biostatistics, Michigan State University, East Lansing, MI, USA. romeror@mail.nih.gov.
  • Gallo DM; Detroit Medical Center, Detroit, MI, USA. romeror@mail.nih.gov.
  • Galaz J; Departamento de Ginecología y Obstetricia, Fundación Valle del Lili, Cali, Colombia.
  • Arenas-Hernandez M; Departamento de Ginecología y Obstetricia, Facultad de Ciencias de la Salud, Universidad Icesi, Cali, Colombia.
  • Bhatti G; Departamento de Ginecología y Obstetricia, Fundación Valle del Lili, Cali, Colombia.
  • Done B; Departamento de Ginecología y Obstetricia, Facultad de Ciencias de la Salud, Universidad Icesi, Cali, Colombia.
  • Zambrano MA; Departamento de Ginecología y Obstetricia, Fundación Valle del Lili, Cali, Colombia.
  • Ramos I; Departamento de Ginecología y Obstetricia, Facultad de Ciencias de la Salud, Universidad Icesi, Cali, Colombia.
  • Fernandez PA; Departamento de Laboratorio Clínico y Patología, Fundación Valle del Lili, Cali, Colombia.
  • Posada L; Facultad de Ciencias de la Salud, Universidad Icesi, Cali, Colombia.
  • Chaiworapongsa T; Centro de Investigaciones Clínicas, Fundación Valle del Lili, Cali, Colombia.
  • Jung E; Pregnancy Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services (NICHD/NIH/DHHS), Detroit, MI,
  • Garcia-Flores V; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
  • Suksai M; Pregnancy Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services (NICHD/NIH/DHHS), Detroit, MI,
  • Gotsch F; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
  • Bosco M; Pregnancy Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services (NICHD/NIH/DHHS), Detroit, MI,
  • Than NG; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.
  • Tarca AL; Division of Obstetrics and Gynecology, School of Medicine, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
Commun Med (Lond) ; 3(1): 48, 2023 Apr 04.
Article en En | MEDLINE | ID: mdl-37016066
ABSTRACT

BACKGROUND:

Pregnant women are at greater risk of adverse outcomes, including mortality, as well as obstetrical complications resulting from COVID-19. However, pregnancy-specific changes that underlie such worsened outcomes remain unclear.

METHODS:

Plasma samples were collected from pregnant women and non-pregnant individuals (male and female) with (n = 72 pregnant, 52 non-pregnant) and without (n = 29 pregnant, 41 non-pregnant) COVID-19. COVID-19 patients were grouped as asymptomatic, mild, moderate, severe, or critically ill according to NIH classifications. Proteomic profiling of 7,288 analytes corresponding to 6,596 unique protein targets was performed using the SOMAmer platform.

RESULTS:

Herein, we profile the plasma proteome of pregnant and non-pregnant COVID-19 patients and controls and show alterations that display a dose-response relationship with disease severity; yet, such proteomic perturbations are dampened during pregnancy. In both pregnant and non-pregnant state, the proteome response induced by COVID-19 shows enrichment of mediators implicated in cytokine storm, endothelial dysfunction, and angiogenesis. Shared and pregnancy-specific proteomic changes are identified pregnant women display a tailored response that may protect the conceptus from heightened inflammation, while non-pregnant individuals display a stronger response to repel infection. Furthermore, the plasma proteome can accurately identify COVID-19 patients, even when asymptomatic or with mild symptoms.

CONCLUSION:

This study represents the most comprehensive characterization of the plasma proteome of pregnant and non-pregnant COVID-19 patients. Our findings emphasize the distinct immune modulation between the non-pregnant and pregnant states, providing insight into the pathogenesis of COVID-19 as well as a potential explanation for the more severe outcomes observed in pregnant women.
Pregnant COVID-19 patients are at increased risk of experiencing complications and severe outcomes compared to the general population. However, the reasons for this heightened risk are still unclear. We measured the proteins present in the blood of pregnant and non-pregnant patients with COVID-19 and compared these to healthy individuals. We found that some COVID-19-associated proteins were present at lower levels in pregnant women, which could help to protect the fetus from harmful inflammation, the body's natural response to infection. While some proteins affected by COVID-19 are shared between pregnant and non-pregnant patients, others were distinctly affected only in pregnant women, providing a potential explanation for the more severe outcomes in this group.

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Commun Med (Lond) Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Commun Med (Lond) Año: 2023 Tipo del documento: Article