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 in | Journal of clinical immunology Vol. 32; no. 2; pp. 300 - 311 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Boston
Springer US
01.04.2012
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Thomas A. surname: Kraus fullname: Kraus, Thomas A. organization: Department of Obstetrics, Gynecology and Reproductive Sciences, Mount Sinai School of Medicine, Department of Microbiology, Mount Sinai School of Medicine – sequence: 2 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 – sequence: 3 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 – sequence: 5 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 – sequence: 6 givenname: Sylvan surname: Wallenstein fullname: Wallenstein, Sylvan organization: Department of Preventive Medicine, Mount Sinai School of Medicine – sequence: 7 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 – sequence: 9 givenname: Tricia surname: Singh fullname: Singh, Tricia organization: Department of Obstetrics, Gynecology and Reproductive Sciences, Mount Sinai School of Medicine – sequence: 10 givenname: Martine surname: Loubeau fullname: Loubeau, Martine organization: Department of Microbiology, Mount Sinai School of Medicine – sequence: 11 givenname: Thomas M. surname: Moran 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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Copyright | Springer Science+Business Media, LLC 2011 Copyright Springer Nature B.V. Apr 2012 |
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Keywords | Pregnancy influenza cytokines immunity gestation Th2 |
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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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