Relationship of Nef-positive and GFAP-reactive astrocytes to drug use in early and late HIV infection
Reactive astrocytosis is a well‐documented feature of HIV encephalitis (HIVE), but it is unclear whether restricted infection of astrocytes contributes to this phenomenon. In addition, the part played by reactive and/or infected astrocytes in AIDS‐related dementia is not fully understood. In this st...
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| Published in | Neuropathology and applied neurobiology Vol. 29; no. 4; pp. 378 - 388 |
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| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
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Oxford, UK
Blackwell Science Ltd
01.08.2003
Blackwell Science |
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| Online Access | Get full text |
| ISSN | 0305-1846 1365-2990 |
| DOI | 10.1046/j.1365-2990.2003.00475.x |
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| Abstract | Reactive astrocytosis is a well‐documented feature of HIV encephalitis (HIVE), but it is unclear whether restricted infection of astrocytes contributes to this phenomenon. In addition, the part played by reactive and/or infected astrocytes in AIDS‐related dementia is not fully understood. In this study of patients at different stages of the human immunodeficiency virus (HIV) infection, who had been treated at most with one antiretroviral drug, reactive astrocytes were identified by immunopositivity for glial fibrillary acidic protein (GFAP) and infected astrocytes by positivity for HIV Nef protein. Results were compared for drug‐using AIDS patients with (n = 9) and without (n = 7) HIVE, for presymptomatic HIV‐positive drug users (n = 12) and for control HIV‐negative subjects (n = 20), including a group who used drugs (n = 10). GFAP‐reactive astrocytes in both grey and white matter were significantly more numerous in HIVE subjects than in each of the other groups but did not correlate with viral load. Nef‐positive astrocytes were confined to HIVE cases and to white matter, but were numerous in only one subject who was treatment‐naive. Nef‐positive microglia were identified in all HIVE cases and in occasional AIDS and presymptomatic subjects who did not have HIVE. The results suggest that astrocytes may form an additional viral reservoir in late HIV infection and may contribute to HIVE. However, the number of GFAP‐positive astrocytes was neither increased in pre‐AIDS nor in drug abuse, in contrast with microglia which we have shown previously to be up‐regulated in both states. |
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| AbstractList | Reactive astrocytosis is a well-documented feature of HIV encephalitis (HIVE), but it is unclear whether restricted infection of astrocytes contributes to this phenomenon. In addition, the part played by reactive and/or infected astrocytes in AIDS-related dementia is not fully understood. In this study of patients at different stages of the human immunodeficiency virus (HIV) infection, who had been treated at most with one antiretroviral drug, reactive astrocytes were identified by immunopositivity for glial fibrillary acidic protein (GFAP) and infected astrocytes by positivity for HIV Nef protein. Results were compared for drug-using AIDS patients with (n=9) and without (n=7) HIVE, for presymptomatic HIV-positive drug users (n=12) and for control HIV-negative subjects (n=20), including a group who used drugs (n=10). GFAP-reactive astrocytes in both grey and white matter were significantly more numerous in HIVE subjects than in each of the other groups but did not correlate with viral load. Nef-positive astrocytes were confined to HIVE cases and to white matter, but were numerous in only one subject who was treatment-naive. Nef-positive microglia were identified in all HIVE cases and in occasional AIDS and presymptomatic subjects who did not have HIVE. The results suggest that astrocytes may form an additional viral reservoir in late HIV infection and may contribute to HIVE. However, the number of GFAP-positive astrocytes was neither increased in pre-AIDS nor in drug abuse, in contrast with microglia which we have shown previously to be up-regulated in both states.Reactive astrocytosis is a well-documented feature of HIV encephalitis (HIVE), but it is unclear whether restricted infection of astrocytes contributes to this phenomenon. In addition, the part played by reactive and/or infected astrocytes in AIDS-related dementia is not fully understood. In this study of patients at different stages of the human immunodeficiency virus (HIV) infection, who had been treated at most with one antiretroviral drug, reactive astrocytes were identified by immunopositivity for glial fibrillary acidic protein (GFAP) and infected astrocytes by positivity for HIV Nef protein. Results were compared for drug-using AIDS patients with (n=9) and without (n=7) HIVE, for presymptomatic HIV-positive drug users (n=12) and for control HIV-negative subjects (n=20), including a group who used drugs (n=10). GFAP-reactive astrocytes in both grey and white matter were significantly more numerous in HIVE subjects than in each of the other groups but did not correlate with viral load. Nef-positive astrocytes were confined to HIVE cases and to white matter, but were numerous in only one subject who was treatment-naive. Nef-positive microglia were identified in all HIVE cases and in occasional AIDS and presymptomatic subjects who did not have HIVE. The results suggest that astrocytes may form an additional viral reservoir in late HIV infection and may contribute to HIVE. However, the number of GFAP-positive astrocytes was neither increased in pre-AIDS nor in drug abuse, in contrast with microglia which we have shown previously to be up-regulated in both states. Reactive astrocytosis is a well-documented feature of HIV encephalitis (HIVE), but it is unclear whether restricted infection of astrocytes contributes to this phenomenon. In addition, the part played by reactive and-or infected astrocytes in AIDS-related dementia is not fully understood. In this study of patients at different stages of the human immunodeficiency virus (HIV) infection, who had been treated at most with one antiretroviral drug, reactive astrocytes were identified by immunopositivity for glial fibrillary acidic protein (GFAP) and infected astrocytes by positivity for HIV Nef protein. Results were compared for drug-using AIDS patients with (n = 9) and without (n = 7) HIVE, for presymptomatic HIV-positive drug users (n = 12) and for control HIV-negative subjects (n = 20), including a group who used drugs (n = 10). GFAP-reactive astrocytes in both grey and white matter were significantly more numerous in HIVE subjects than in each of the other groups but did not correlate with viral load. Nef-positive astrocytes were confined to HIVE cases and to white matter, but were numerous in only one subject who was treatment-naive. Nef-positive microglia were identified in all HIVE cases and in occasional AIDS and presymptomatic subjects who did not have HIVE. The results suggest that astrocytes may form an additional viral reservoir in late HIV infection and may contribute to HIVE. However, the number of GFAP-positive astrocytes was neither increased in pre-AIDS nor in drug abuse, in contrast with microglia which we have shown previously to be up-regulated in both states. Reactive astrocytosis is a well‐documented feature of HIV encephalitis (HIVE), but it is unclear whether restricted infection of astrocytes contributes to this phenomenon. In addition, the part played by reactive and/or infected astrocytes in AIDS‐related dementia is not fully understood. In this study of patients at different stages of the human immunodeficiency virus (HIV) infection, who had been treated at most with one antiretroviral drug, reactive astrocytes were identified by immunopositivity for glial fibrillary acidic protein (GFAP) and infected astrocytes by positivity for HIV Nef protein. Results were compared for drug‐using AIDS patients with ( n = 9) and without ( n = 7) HIVE, for presymptomatic HIV‐positive drug users ( n = 12) and for control HIV‐negative subjects ( n = 20), including a group who used drugs ( n = 10). GFAP‐reactive astrocytes in both grey and white matter were significantly more numerous in HIVE subjects than in each of the other groups but did not correlate with viral load. Nef‐positive astrocytes were confined to HIVE cases and to white matter, but were numerous in only one subject who was treatment‐naive. Nef‐positive microglia were identified in all HIVE cases and in occasional AIDS and presymptomatic subjects who did not have HIVE. The results suggest that astrocytes may form an additional viral reservoir in late HIV infection and may contribute to HIVE. However, the number of GFAP‐positive astrocytes was neither increased in pre‐AIDS nor in drug abuse, in contrast with microglia which we have shown previously to be up‐regulated in both states. |
| Author | Tomlinson, G. S. Anderson, C. E. Pauly, B. Brannan, F. W. Chiswick, A. Bell, J. E. Brack-Werner, R. Simmonds, P. |
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| Keywords | restricted infection drug abuse HIV Nef protein HIV-associated dementia AIDS astrocyte glial fibrillary acidic protein |
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| Snippet | Reactive astrocytosis is a well‐documented feature of HIV encephalitis (HIVE), but it is unclear whether restricted infection of astrocytes contributes to this... Reactive astrocytosis is a well-documented feature of HIV encephalitis (HIVE), but it is unclear whether restricted infection of astrocytes contributes to this... |
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| SubjectTerms | Adult AIDS AIDS Dementia Complex - complications AIDS Dementia Complex - metabolism AIDS Dementia Complex - pathology astrocyte Astrocytes - chemistry Astrocytes - pathology Astrocytes - virology Biological and medical sciences Cell Count Cognition Disorders - metabolism Cognition Disorders - pathology Cognition Disorders - virology drug abuse Female Gene Products, nef - analysis glial fibrillary acidic protein Glial Fibrillary Acidic Protein - analysis Gliosis - metabolism Gliosis - pathology Gliosis - virology HIV HIV-associated dementia Human immunodeficiency virus Humans Immunohistochemistry Male Medical sciences Middle Aged nef Gene Products, Human Immunodeficiency Virus Nef protein Proviruses restricted infection Substance-Related Disorders - complications Substance-Related Disorders - pathology Viral Load |
| Title | Relationship of Nef-positive and GFAP-reactive astrocytes to drug use in early and late HIV infection |
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