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Persistence of Antibody to Human Parvovirus B19 After Allogeneic Bone Marrow Transplantation: Role of Prior Recipient Immunity

Human parvovirus B19 (B19) IgG was studied retrospectively in 66 allogeneic bone marrow transplantation (BMT) patients using an enzyme-linked immunosorbent assay. Recipient and donor sera had been stored pre-BMT together with sequential sera thereafter. Approximately half of donors and recipients ha...

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Published in:Blood 1997-06, Vol.89 (12), p.4646-4651
Main Authors: Ang, H.A., Apperley, J.F., Ward, K.N.
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description Human parvovirus B19 (B19) IgG was studied retrospectively in 66 allogeneic bone marrow transplantation (BMT) patients using an enzyme-linked immunosorbent assay. Recipient and donor sera had been stored pre-BMT together with sequential sera thereafter. Approximately half of donors and recipients had anti-B19 IgG pre-BMT and thus the relative contributions of donor and recipient immunity to antibody production after transplantation could be assessed. For each patient, a serum taken 2 to 3 years after BMT was also tested and the results show that persistence of B19 antibody depends on prior recipient (P = .0003) but not on donor immunity (P = .8). The findings were similar in both sibling and (VUD) BMT volunteer unrelated donor patients. Analysis of sequential post-BMT sera from 41 of the patients, for whom appropriately timed samples were available, showed primary B19 infection in 3 seronegative individuals, whereas 5 others who were seropositive before BMT underwent recurrent infection. Sequential results from the remaining 33 patients without recent B19 infection showed no evidence for donor antibody transfer and confirmed that antibody persistence depends on prior recipient immunity. B19 IgG levels decreased variably with time and some patients eventually became seronegative. It is concluded that this long-term persistence of B19 antibody post-BMT is most probably due to the existence of long-lived recipient plasma cells.
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Recipient and donor sera had been stored pre-BMT together with sequential sera thereafter. Approximately half of donors and recipients had anti-B19 IgG pre-BMT and thus the relative contributions of donor and recipient immunity to antibody production after transplantation could be assessed. For each patient, a serum taken 2 to 3 years after BMT was also tested and the results show that persistence of B19 antibody depends on prior recipient (P = .0003) but not on donor immunity (P = .8). The findings were similar in both sibling and (VUD) BMT volunteer unrelated donor patients. Analysis of sequential post-BMT sera from 41 of the patients, for whom appropriately timed samples were available, showed primary B19 infection in 3 seronegative individuals, whereas 5 others who were seropositive before BMT underwent recurrent infection. Sequential results from the remaining 33 patients without recent B19 infection showed no evidence for donor antibody transfer and confirmed that antibody persistence depends on prior recipient immunity. B19 IgG levels decreased variably with time and some patients eventually became seronegative. It is concluded that this long-term persistence of B19 antibody post-BMT is most probably due to the existence of long-lived recipient plasma cells.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.V89.12.4646</identifier><identifier>PMID: 9192791</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Adult ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Antibodies, Viral - blood ; Biological and medical sciences ; Bone Marrow Transplantation - adverse effects ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Enzyme-Linked Immunosorbent Assay ; Female ; Follow-Up Studies ; Humans ; Immunosuppression ; Leukemia - complications ; Leukemia - therapy ; Male ; Medical sciences ; Middle Aged ; Myelodysplastic Syndromes - complications ; Myelodysplastic Syndromes - therapy ; Parvoviridae Infections - epidemiology ; Parvoviridae Infections - immunology ; Parvoviridae Infections - transmission ; Parvovirus B19, Human - immunology ; Parvovirus B19, Human - isolation &amp; purification ; Plasma Cells - immunology ; Prevalence ; Recurrence ; Retrospective Studies ; Seroepidemiologic Studies ; Transfusions. Complications. Transfusion reactions. 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Recipient and donor sera had been stored pre-BMT together with sequential sera thereafter. Approximately half of donors and recipients had anti-B19 IgG pre-BMT and thus the relative contributions of donor and recipient immunity to antibody production after transplantation could be assessed. For each patient, a serum taken 2 to 3 years after BMT was also tested and the results show that persistence of B19 antibody depends on prior recipient (P = .0003) but not on donor immunity (P = .8). The findings were similar in both sibling and (VUD) BMT volunteer unrelated donor patients. Analysis of sequential post-BMT sera from 41 of the patients, for whom appropriately timed samples were available, showed primary B19 infection in 3 seronegative individuals, whereas 5 others who were seropositive before BMT underwent recurrent infection. Sequential results from the remaining 33 patients without recent B19 infection showed no evidence for donor antibody transfer and confirmed that antibody persistence depends on prior recipient immunity. B19 IgG levels decreased variably with time and some patients eventually became seronegative. It is concluded that this long-term persistence of B19 antibody post-BMT is most probably due to the existence of long-lived recipient plasma cells.</description><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Antibodies, Viral - blood</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Transplantation - adverse effects</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunosuppression</subject><subject>Leukemia - complications</subject><subject>Leukemia - therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myelodysplastic Syndromes - complications</subject><subject>Myelodysplastic Syndromes - therapy</subject><subject>Parvoviridae Infections - epidemiology</subject><subject>Parvoviridae Infections - immunology</subject><subject>Parvoviridae Infections - transmission</subject><subject>Parvovirus B19, Human - immunology</subject><subject>Parvovirus B19, Human - isolation &amp; purification</subject><subject>Plasma Cells - immunology</subject><subject>Prevalence</subject><subject>Recurrence</subject><subject>Retrospective Studies</subject><subject>Seroepidemiologic Studies</subject><subject>Transfusions. 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Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Antibodies, Viral - blood</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Transplantation - adverse effects</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunosuppression</topic><topic>Leukemia - complications</topic><topic>Leukemia - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myelodysplastic Syndromes - complications</topic><topic>Myelodysplastic Syndromes - therapy</topic><topic>Parvoviridae Infections - epidemiology</topic><topic>Parvoviridae Infections - immunology</topic><topic>Parvoviridae Infections - transmission</topic><topic>Parvovirus B19, Human - immunology</topic><topic>Parvovirus B19, Human - isolation &amp; purification</topic><topic>Plasma Cells - immunology</topic><topic>Prevalence</topic><topic>Recurrence</topic><topic>Retrospective Studies</topic><topic>Seroepidemiologic Studies</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Transplantation Conditioning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ang, H.A.</creatorcontrib><creatorcontrib>Apperley, J.F.</creatorcontrib><creatorcontrib>Ward, K.N.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ang, H.A.</au><au>Apperley, J.F.</au><au>Ward, K.N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Persistence of Antibody to Human Parvovirus B19 After Allogeneic Bone Marrow Transplantation: Role of Prior Recipient Immunity</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>1997-06-15</date><risdate>1997</risdate><volume>89</volume><issue>12</issue><spage>4646</spage><epage>4651</epage><pages>4646-4651</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Human parvovirus B19 (B19) IgG was studied retrospectively in 66 allogeneic bone marrow transplantation (BMT) patients using an enzyme-linked immunosorbent assay. Recipient and donor sera had been stored pre-BMT together with sequential sera thereafter. Approximately half of donors and recipients had anti-B19 IgG pre-BMT and thus the relative contributions of donor and recipient immunity to antibody production after transplantation could be assessed. For each patient, a serum taken 2 to 3 years after BMT was also tested and the results show that persistence of B19 antibody depends on prior recipient (P = .0003) but not on donor immunity (P = .8). The findings were similar in both sibling and (VUD) BMT volunteer unrelated donor patients. Analysis of sequential post-BMT sera from 41 of the patients, for whom appropriately timed samples were available, showed primary B19 infection in 3 seronegative individuals, whereas 5 others who were seropositive before BMT underwent recurrent infection. Sequential results from the remaining 33 patients without recent B19 infection showed no evidence for donor antibody transfer and confirmed that antibody persistence depends on prior recipient immunity. B19 IgG levels decreased variably with time and some patients eventually became seronegative. It is concluded that this long-term persistence of B19 antibody post-BMT is most probably due to the existence of long-lived recipient plasma cells.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>9192791</pmid><doi>10.1182/blood.V89.12.4646</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Antibodies, Viral - blood
Biological and medical sciences
Bone Marrow Transplantation - adverse effects
Bone marrow, stem cells transplantation. Graft versus host reaction
Enzyme-Linked Immunosorbent Assay
Female
Follow-Up Studies
Humans
Immunosuppression
Leukemia - complications
Leukemia - therapy
Male
Medical sciences
Middle Aged
Myelodysplastic Syndromes - complications
Myelodysplastic Syndromes - therapy
Parvoviridae Infections - epidemiology
Parvoviridae Infections - immunology
Parvoviridae Infections - transmission
Parvovirus B19, Human - immunology
Parvovirus B19, Human - isolation & purification
Plasma Cells - immunology
Prevalence
Recurrence
Retrospective Studies
Seroepidemiologic Studies
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transplantation Conditioning
title Persistence of Antibody to Human Parvovirus B19 After Allogeneic Bone Marrow Transplantation: Role of Prior Recipient Immunity
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