Characterizing the Pregnancy Immune Phenotype: Results of the Viral Immunity and Pregnancy (VIP) Study

Purpose The increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune diseases support the existence of pregnancy-related alterations in immune status. Elucidating the changes in innate and adaptive immunit...

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Published inJournal of clinical immunology Vol. 32; no. 2; pp. 300 - 311
Main Authors Kraus, Thomas A., Engel, Stephanie M., Sperling, Rhoda S., Kellerman, Lisa, Lo, Yungtai, Wallenstein, Sylvan, Escribese, Maria M., Garrido, Jose L., Singh, Tricia, Loubeau, Martine, Moran, Thomas M.
Format Journal Article
LanguageEnglish
Published Boston Springer US 01.04.2012
Springer Nature B.V
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Abstract Purpose The increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune diseases support the existence of pregnancy-related alterations in immune status. Elucidating the changes in innate and adaptive immunity during gestation may improve pregnancy outcomes and facilitate the development of targeted therapies for autoimmune diseases. Method The Viral Immunity and Pregnancy (VIP) study evaluated over 50 subjects longitudinally at three time points during pregnancy and at two time points post-delivery. Leukocyte enumeration was performed; functional responses of NK cells and CD4 T cells were analyzed, and soluble factors such as cytokines, defensins, and steroid hormones were measured in maternal blood. Results In comparison to the post-partum period, the latter part of pregnancy was characterized by significant increases in blood phagocytes and pDCs and decreases in the number and activity of NK and T cells. Alterations were found in antimicrobial proteins and serum cytokines. Conclusions These data show that pregnancy is not a period of immunosuppression but an alteration in immune priorities characterized by a strengthening of innate immune barriers and a concomitant reduction in adaptive/inflammatory immunity in the later stages of pregnancy.
AbstractList The increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune diseases support the existence of pregnancy-related alterations in immune status. Elucidating the changes in innate and adaptive immunity during gestation may improve pregnancy outcomes and facilitate the development of targeted therapies for autoimmune diseases. The Viral Immunity and Pregnancy (VIP) study evaluated over 50 subjects longitudinally at three time points during pregnancy and at two time points post-delivery. Leukocyte enumeration was performed; functional responses of NK cells and CD4 T cells were analyzed, and soluble factors such as cytokines, defensins, and steroid hormones were measured in maternal blood. In comparison to the post-partum period, the latter part of pregnancy was characterized by significant increases in blood phagocytes and pDCs and decreases in the number and activity of NK and T cells. Alterations were found in antimicrobial proteins and serum cytokines. These data show that pregnancy is not a period of immunosuppression but an alteration in immune priorities characterized by a strengthening of innate immune barriers and a concomitant reduction in adaptive/inflammatory immunity in the later stages of pregnancy.
Purpose: The increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune diseases support the existence of pregnancy-related alterations in immune status. Elucidating the changes in innate and adaptive immunity during gestation may improve pregnancy outcomes and facilitate the development of targeted therapies for autoimmune diseases. Method: The Viral Immunity and Pregnancy (VIP) study evaluated over 50 subjects longitudinally at three time points during pregnancy and at two time points post-delivery. Leukocyte enumeration was performed; functional responses of NK cells and CD4 T cells were analyzed, and soluble factors such as cytokines, defensins, and steroid hormones were measured in maternal blood. Results: In comparison to the post-partum period, the latter part of pregnancy was characterized by significant increases in blood phagocytes and pDCs and decreases in the number and activity of NK and T cells. Alterations were found in antimicrobial proteins and serum cytokines. Conclusions: These data show that pregnancy is not a period of immunosuppression but an alteration in immune priorities characterized by a strengthening of innate immune barriers and a concomitant reduction in adaptive/inflammatory immunity in the later stages of pregnancy.
Purpose The increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune diseases support the existence of pregnancy-related alterations in immune status. Elucidating the changes in innate and adaptive immunity during gestation may improve pregnancy outcomes and facilitate the development of targeted therapies for autoimmune diseases. Method The Viral Immunity and Pregnancy (VIP) study evaluated over 50 subjects longitudinally at three time points during pregnancy and at two time points post-delivery. Leukocyte enumeration was performed; functional responses of NK cells and CD4 T cells were analyzed, and soluble factors such as cytokines, defensins, and steroid hormones were measured in maternal blood. Results In comparison to the post-partum period, the latter part of pregnancy was characterized by significant increases in blood phagocytes and pDCs and decreases in the number and activity of NK and T cells. Alterations were found in antimicrobial proteins and serum cytokines. Conclusions These data show that pregnancy is not a period of immunosuppression but an alteration in immune priorities characterized by a strengthening of innate immune barriers and a concomitant reduction in adaptive/inflammatory immunity in the later stages of pregnancy.
PurposeThe increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune diseases support the existence of pregnancy-related alterations in immune status. Elucidating the changes in innate and adaptive immunity during gestation may improve pregnancy outcomes and facilitate the development of targeted therapies for autoimmune diseases.MethodThe Viral Immunity and Pregnancy (VIP) study evaluated over 50 subjects longitudinally at three time points during pregnancy and at two time points post-delivery. Leukocyte enumeration was performed; functional responses of NK cells and CD4 T cells were analyzed, and soluble factors such as cytokines, defensins, and steroid hormones were measured in maternal blood.ResultsIn comparison to the post-partum period, the latter part of pregnancy was characterized by significant increases in blood phagocytes and pDCs and decreases in the number and activity of NK and T cells. Alterations were found in antimicrobial proteins and serum cytokines.ConclusionsThese data show that pregnancy is not a period of immunosuppression but an alteration in immune priorities characterized by a strengthening of innate immune barriers and a concomitant reduction in adaptive/inflammatory immunity in the later stages of pregnancy.
The increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune diseases support the existence of pregnancy-related alterations in immune status. Elucidating the changes in innate and adaptive immunity during gestation may improve pregnancy outcomes and facilitate the development of targeted therapies for autoimmune diseases.PURPOSEThe increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune diseases support the existence of pregnancy-related alterations in immune status. Elucidating the changes in innate and adaptive immunity during gestation may improve pregnancy outcomes and facilitate the development of targeted therapies for autoimmune diseases.The Viral Immunity and Pregnancy (VIP) study evaluated over 50 subjects longitudinally at three time points during pregnancy and at two time points post-delivery. Leukocyte enumeration was performed; functional responses of NK cells and CD4 T cells were analyzed, and soluble factors such as cytokines, defensins, and steroid hormones were measured in maternal blood.METHODThe Viral Immunity and Pregnancy (VIP) study evaluated over 50 subjects longitudinally at three time points during pregnancy and at two time points post-delivery. Leukocyte enumeration was performed; functional responses of NK cells and CD4 T cells were analyzed, and soluble factors such as cytokines, defensins, and steroid hormones were measured in maternal blood.In comparison to the post-partum period, the latter part of pregnancy was characterized by significant increases in blood phagocytes and pDCs and decreases in the number and activity of NK and T cells. Alterations were found in antimicrobial proteins and serum cytokines.RESULTSIn comparison to the post-partum period, the latter part of pregnancy was characterized by significant increases in blood phagocytes and pDCs and decreases in the number and activity of NK and T cells. Alterations were found in antimicrobial proteins and serum cytokines.These data show that pregnancy is not a period of immunosuppression but an alteration in immune priorities characterized by a strengthening of innate immune barriers and a concomitant reduction in adaptive/inflammatory immunity in the later stages of pregnancy.CONCLUSIONSThese data show that pregnancy is not a period of immunosuppression but an alteration in immune priorities characterized by a strengthening of innate immune barriers and a concomitant reduction in adaptive/inflammatory immunity in the later stages of pregnancy.
Author Moran, Thomas M.
Engel, Stephanie M.
Wallenstein, Sylvan
Lo, Yungtai
Kraus, Thomas A.
Escribese, Maria M.
Garrido, Jose L.
Sperling, Rhoda S.
Kellerman, Lisa
Singh, Tricia
Loubeau, Martine
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  givenname: Stephanie M.
  surname: Engel
  fullname: Engel, Stephanie M.
  organization: Department of Preventive Medicine, Mount Sinai School of Medicine, Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill
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  givenname: Rhoda S.
  surname: Sperling
  fullname: Sperling, Rhoda S.
  organization: Department of Obstetrics, Gynecology and Reproductive Sciences, Mount Sinai School of Medicine
– sequence: 4
  givenname: Lisa
  surname: Kellerman
  fullname: Kellerman, Lisa
  organization: Department of Preventive Medicine, Mount Sinai School of Medicine
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  givenname: Yungtai
  surname: Lo
  fullname: Lo, Yungtai
  organization: Department of Preventive Medicine, Mount Sinai School of Medicine, Department of Epidemiology and Population Health, Albert Einstein College of Medicine
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  givenname: Sylvan
  surname: Wallenstein
  fullname: Wallenstein, Sylvan
  organization: Department of Preventive Medicine, Mount Sinai School of Medicine
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  givenname: Maria M.
  surname: Escribese
  fullname: Escribese, Maria M.
  organization: Department of Microbiology, Mount Sinai School of Medicine, Department of Molecular Microbiology and Infections Biology, CIB, CSIC
– sequence: 8
  givenname: Jose L.
  surname: Garrido
  fullname: Garrido, Jose L.
  organization: Department of Microbiology, Mount Sinai School of Medicine
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  givenname: Tricia
  surname: Singh
  fullname: Singh, Tricia
  organization: Department of Obstetrics, Gynecology and Reproductive Sciences, Mount Sinai School of Medicine
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  fullname: Moran, Thomas M.
  email: Thomas.Moran@mssm.edu
  organization: Department of Microbiology, Mount Sinai School of Medicine
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22198680$$D View this record in MEDLINE/PubMed
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Issue 2
Keywords Pregnancy
influenza
cytokines
immunity
gestation
Th2
Language English
License This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
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The increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some autoimmune...
PurposeThe increased risk of morbidity and mortality from certain microbial infections and the demonstrated improvements in the clinical course of some...
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SubjectTerms Adaptive Immunity
Adult
Antimicrobial agents
Autoimmune diseases
Biomedical and Life Sciences
Biomedicine
Blood
CD4 antigen
Cytokines
Data processing
Defensins
Enumeration
Female
Gestation
Humans
Immune status
Immunity
Immunity, Innate
Immunology
Immunophenotyping
Immunosuppression
Infection
Infectious Diseases
Inflammation
Internal Medicine
Leukocytes
Leukocytes - immunology
Leukocytes - metabolism
Lymphocytes T
Medical Microbiology
Morbidity
Mortality
Natural killer cells
Phagocytes
Phenotype
Phenotypes
Pregnancy
Pregnancy Complications, Infectious - immunology
Serum - chemistry
Steroid hormones
Vasoactive intestinal peptide
Young Adult
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Title Characterizing the Pregnancy Immune Phenotype: Results of the Viral Immunity and Pregnancy (VIP) Study
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Volume 32
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