Literature DB >> 15041161

HLA class I noninherited maternal antigens in cord blood and breast milk.

Melanie L Molitor1, Lynn D Haynes, Ewa Jankowska-Gan, Arend Mulder, William J Burlingham.   

Abstract

Maternally induced allotolerance both in clinical and experimental organ transplantation appears to require both in utero and oral exposure to noninherited maternal antigens (NIMA). Soluble major histocompatibility complex (MHC) class I antigens were studied in 18 mother-baby pairs in order to determine the extent of neonatal exposure to NIMA. Enzyme-linked immunoabsorbent assay (ELISA) analysis of cord blood from three genetically HLA-A2 negative babies born to HLA-A2+ mothers and from two HLA-A3 negative babies born to HLA-A3+ mothers revealed significant NIMA HLA-A levels in cord plasma. The level of NIMA-A2 or -A3 in cord blood were approximately 10% of the predicted value for a baby genetically positive for that allele. HLA-A2 or -A3 was undetectable (< 1.0 ng/ml) in cord blood from HLA-A2 or -A3 negative babies whose mothers were also HLA-A2 or -A3 negative. Breast milk from HLA-A2+ mothers contained soluble HLA-A2 (sHLA-A2) at levels averaging 36.2 ng/ml, resulting in milligram quantities of ingested antigen over 3 months of nursing. Western blot analysis of cord plasma confirmed that bands corresponding to NIMA HLA-A protein were present. This study demonstrates that oral and intravenous exposure to NIMA sHLA in the fetus and newborn is much higher than previously thought, and emphasizes the importance of nursing in the overall antigen dose achieved.

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Year:  2004        PMID: 15041161     DOI: 10.1016/j.humimm.2003.12.006

Source DB:  PubMed          Journal:  Hum Immunol        ISSN: 0198-8859            Impact factor:   2.850


  17 in total

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Authors:  Shannon J Opiela; Becky Adkins
Journal:  Chimerism       Date:  2010 Jul-Sep

2.  Breast milk and transplantation tolerance.

Authors:  Kazutoshi Aoyama; Ken-Ichi Matsuoka; Takanori Teshima
Journal:  Chimerism       Date:  2010 Jul-Sep

Review 3.  Immunological implications of pregnancy-induced microchimerism.

Authors:  Jeremy M Kinder; Ina A Stelzer; Petra C Arck; Sing Sing Way
Journal:  Nat Rev Immunol       Date:  2017-05-08       Impact factor: 53.106

Review 4.  Microchimerism: tolerance vs. sensitization.

Authors:  Partha Dutta; William J Burlingham
Journal:  Curr Opin Organ Transplant       Date:  2011-08       Impact factor: 2.640

5.  Stem cell microchimerism and tolerance to non-inherited maternal antigens.

Authors:  Partha Dutta; William J Burlingham
Journal:  Chimerism       Date:  2010 Jul-Sep

Review 6.  Tolerance to noninherited maternal antigens in mice and humans.

Authors:  Partha Dutta; William J Burlingham
Journal:  Curr Opin Organ Transplant       Date:  2009-08       Impact factor: 2.640

7.  Microchimerism is strongly correlated with tolerance to noninherited maternal antigens in mice.

Authors:  Partha Dutta; Melanie Molitor-Dart; Joseph L Bobadilla; Drew A Roenneburg; Zhen Yan; Jose R Torrealba; William J Burlingham
Journal:  Blood       Date:  2009-08-21       Impact factor: 22.113

8.  Cross-Generational Reproductive Fitness Enforced by Microchimeric Maternal Cells.

Authors:  Jeremy M Kinder; Tony T Jiang; James M Ertelt; Lijun Xin; Beverly S Strong; Aimen F Shaaban; Sing Sing Way
Journal:  Cell       Date:  2015-07-23       Impact factor: 41.582

9.  Murine neonates develop vigorous in vivo cytotoxic and Th1/Th2 responses upon exposure to low doses of NIMA-like alloantigens.

Authors:  Shannon J Opiela; Robert B Levy; Becky Adkins
Journal:  Blood       Date:  2008-06-06       Impact factor: 22.113

10.  Chimeric maternal cells with tissue-specific antigen expression and morphology are common in infant tissues.

Authors:  Anne M Stevens; Heidi M Hermes; Meghan M Kiefer; Joe C Rutledge; J Lee Nelson
Journal:  Pediatr Dev Pathol       Date:  2009 Sep-Oct
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