Effectiveness of RSVIG prophylaxis and therapy of respiratory syncytial virus in an immunosuppressed animal model

Respiratory syncytial virus (RSV) has emerged as a leading cause of pneumonia, with high mortality, in bone marrow transplant (BMT) recipients, as well as in other profoundly immunocompromised patients, such as myelosuppressed adults with leukemia. We tested the efficacy of immunoglobulin with high...

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Published in:Bone marrow transplantation (Basingstoke) Vol. 24; no. 1; pp. 41 - 45
Main Authors: OTTOLINI, M. G, PORTER, D. D, HEMMING, V. G, ZIMMERMAN, M. N, SCHWAB, N. M, PRINCE, G. A
Format: Journal Article
Language:English
Published: Basingstoke Nature Publishing Group 01-07-1999
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Abstract Respiratory syncytial virus (RSV) has emerged as a leading cause of pneumonia, with high mortality, in bone marrow transplant (BMT) recipients, as well as in other profoundly immunocompromised patients, such as myelosuppressed adults with leukemia. We tested the efficacy of immunoglobulin with high anti-RSV neutralizing antibody levels (RSVIG) for prophylaxis and therapy of RSV infection in cotton rats undergoing prolonged immunosuppression with cyclophosphamide. These animals experience persistent infection, a model which is similar to the disease seen in post-BMT humans. Both prophylaxis and therapy reduced pulmonary viral replication over 500-fold to nearly undetectable levels. In animals receiving continual immunosuppression, the use of multiple therapeutic doses of RSVIG was able to prevent rebound viral replication, though virus was not completely eliminated.
AbstractList Respiratory syncytial virus (RSV) has emerged as a leading cause of pneumonia, with high mortality, in bone marrow transplant (BMT) recipients, as well as in other profoundly immunocompromised patients, such as myelosuppressed adults with leukemia. We tested the efficacy of immunoglobulin with high anti-RSV neutralizing antibody levels (RSVIG) for prophylaxis and therapy of RSV infection in cotton rats undergoing prolonged immunosuppression with cyclophosphamide. These animals experience persistent infection, a model which is similar to the disease seen in post-BMT humans. Both prophylaxis and therapy reduced pulmonary viral replication over 500-fold to nearly undetectable levels. In animals receiving continual immunosuppression, the use of multiple therapeutic doses of RSVIG was able to prevent rebound viral replication, though virus was not completely eliminated.
Author PRINCE, G. A
OTTOLINI, M. G
SCHWAB, N. M
PORTER, D. D
HEMMING, V. G
ZIMMERMAN, M. N
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Keywords Animal model
Pneumonia
Rat
Spumavirinae
Prevention
Immunotherapy
Bone marrow
Complication
Graft
Immunopathology
Lung disease
Immunoglobulins
Respiratory disease
Treatment efficiency
Rodentia
Retroviridae
Immune deficiency
Infection
Virus
Immunoprophylaxis
Vertebrata
Immunosuppression
Mammalia
Human syncytial virus
Animal
Viral disease
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Snippet Respiratory syncytial virus (RSV) has emerged as a leading cause of pneumonia, with high mortality, in bone marrow transplant (BMT) recipients, as well as in...
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SubjectTerms Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Animals
Antibodies, Viral - therapeutic use
Biological and medical sciences
Bone marrow, stem cells transplantation. Graft versus host reaction
Cyclophosphamide - pharmacology
Disease Models, Animal
Dose-Response Relationship, Immunologic
Immunoglobulins, Intravenous - adverse effects
Immunoglobulins, Intravenous - therapeutic use
Immunosuppressive Agents - adverse effects
Immunosuppressive Agents - therapeutic use
Lung - virology
Medical sciences
Nose - virology
Rats
Rats, Inbred Strains
Respiratory syncytial virus
Respiratory Syncytial Virus Infections - prevention & control
Respiratory Syncytial Viruses - growth & development
Respiratory Syncytial Viruses - immunology
Sigmodontinae
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Virus Replication
Title Effectiveness of RSVIG prophylaxis and therapy of respiratory syncytial virus in an immunosuppressed animal model
URI https://www.ncbi.nlm.nih.gov/pubmed/10435733
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Volume 24
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