Aids-associated vacuolar myelopathy and tumor necrosis factor-alpha (TNFα)

The spinal cords from 15 patients with AIDS-associated vacuolar myelopathy (VM), 4 AIDS patients without VM, and 5 HIV-seronegative controls, were studied with immunocytochemistry for TNFα. CSF and blood from HIV-seropositive patients with VM ( n = 16), non-vacuolar myelopathies ( n = 8), CNS infect...

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Veröffentlicht in:Journal of the neurological sciences 1996-06, Vol.138 (1), p.134-144
Hauptverfasser: Tan, S.V., Guiloff, R.J., Henderson, D.C., Gazzard, B.G., Miller, R.
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container_end_page 144
container_issue 1
container_start_page 134
container_title Journal of the neurological sciences
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creator Tan, S.V.
Guiloff, R.J.
Henderson, D.C.
Gazzard, B.G.
Miller, R.
description The spinal cords from 15 patients with AIDS-associated vacuolar myelopathy (VM), 4 AIDS patients without VM, and 5 HIV-seronegative controls, were studied with immunocytochemistry for TNFα. CSF and blood from HIV-seropositive patients with VM ( n = 16), non-vacuolar myelopathies ( n = 8), CNS infection but no clinical myelopathy ( n = 31), no clinical or radiological evidence of CNS disease ( n = 9), and from 7 HIV-seronegative controls with motor neurone disease were assayed for TNFα using an ELISA technique. TNFα was present on immunostaining in all the 15 cords with VM studied. The stained cells were macrophages, microglia and endothelial cells. The amount of immunostaining was higher in cords with VM compared with cords from HIV-seropositive patients without VM ( p = 0.001). The distribution of staining corresponded to the areas of pathology but did not correlate with the severity of the VM. Immunostaining was also higher in the HIV-seropositive group compared to the HIV-seronegative controls ( p = 0.001). There was no significant difference in the levels of TNFα in the CSF of patients with VM compared to any of the other groups studied. Blood levels of TNFα were lower in the HIV-seropositive controls without CNS disease and in the HIV-seronegative MND controls, than in patients with VM, non-vacuolar myelopathies, and CNS disease. CSF TNFα levels did not appear to be a reliable indicator of intramedullary levels. The findings support the hypothesis that TNFα may be relevant in the pathogenesis of vacuolar change in VM.
doi_str_mv 10.1016/0022-510X(95)00354-5
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CSF and blood from HIV-seropositive patients with VM ( n = 16), non-vacuolar myelopathies ( n = 8), CNS infection but no clinical myelopathy ( n = 31), no clinical or radiological evidence of CNS disease ( n = 9), and from 7 HIV-seronegative controls with motor neurone disease were assayed for TNFα using an ELISA technique. TNFα was present on immunostaining in all the 15 cords with VM studied. The stained cells were macrophages, microglia and endothelial cells. The amount of immunostaining was higher in cords with VM compared with cords from HIV-seropositive patients without VM ( p = 0.001). The distribution of staining corresponded to the areas of pathology but did not correlate with the severity of the VM. Immunostaining was also higher in the HIV-seropositive group compared to the HIV-seronegative controls ( p = 0.001). There was no significant difference in the levels of TNFα in the CSF of patients with VM compared to any of the other groups studied. Blood levels of TNFα were lower in the HIV-seropositive controls without CNS disease and in the HIV-seronegative MND controls, than in patients with VM, non-vacuolar myelopathies, and CNS disease. CSF TNFα levels did not appear to be a reliable indicator of intramedullary levels. 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CSF and blood from HIV-seropositive patients with VM ( n = 16), non-vacuolar myelopathies ( n = 8), CNS infection but no clinical myelopathy ( n = 31), no clinical or radiological evidence of CNS disease ( n = 9), and from 7 HIV-seronegative controls with motor neurone disease were assayed for TNFα using an ELISA technique. TNFα was present on immunostaining in all the 15 cords with VM studied. The stained cells were macrophages, microglia and endothelial cells. The amount of immunostaining was higher in cords with VM compared with cords from HIV-seropositive patients without VM ( p = 0.001). The distribution of staining corresponded to the areas of pathology but did not correlate with the severity of the VM. Immunostaining was also higher in the HIV-seropositive group compared to the HIV-seronegative controls ( p = 0.001). There was no significant difference in the levels of TNFα in the CSF of patients with VM compared to any of the other groups studied. Blood levels of TNFα were lower in the HIV-seropositive controls without CNS disease and in the HIV-seronegative MND controls, than in patients with VM, non-vacuolar myelopathies, and CNS disease. CSF TNFα levels did not appear to be a reliable indicator of intramedullary levels. 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Immunoglobulinopathies</subject><subject>Immunohistochemistry</subject><subject>Immunopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Motor Neuron Disease - immunology</subject><subject>Myelin Sheath - pathology</subject><subject>Myelopathy</subject><subject>Paraparesis</subject><subject>Paraparesis, Tropical Spastic - complications</subject><subject>Paraparesis, Tropical Spastic - metabolism</subject><subject>Paraparesis, Tropical Spastic - pathology</subject><subject>Spinal cord disease</subject><subject>Spinal Cord Diseases - complications</subject><subject>Spinal Cord Diseases - metabolism</subject><subject>Spinal Cord Diseases - pathology</subject><subject>TNF</subject><subject>Tumor Necrosis Factor-alpha - analysis</subject><subject>Tumor Necrosis Factor-alpha - cerebrospinal fluid</subject><subject>Vacuoles - pathology</subject><issn>0022-510X</issn><issn>1878-5883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM9qFEEQhxtR4ib6BgpzEEkOE7u6p6d7L4EQjIohXiJ4a2prqknL_Fm7ZwL7WL6Iz-ROdtljcqpDfb8fVZ8Q70Ceg4T6k5RKlQbkr9OlOZNSm6o0L8QCnHWlcU6_FIsD8loc5_xbSlk7tzwSR84uQRlYiO-Xsckl5jxQxJGb4gFpGlpMRbfhdljjeL8psG-KceqGVPRMacgxFwFpHFKJ7foei9O72-t_f8_eiFcB28xv9_NE_Lz-fHf1tbz58eXb1eVNSRXYsawVAwZWtrGBZOOU0nVgzZaClZrB1azNioyGCqAiQ87KAAEVkVsZVPpEfNz1rtPwZ-I8-i5m4rbFnocpe-u0rGtpngXBOKsqmMFqB87f5cTBr1PsMG08SD_L9rNJP5v0S-MfZfs59n7fP606bg6hvd3t_sN-j5mwDQl7ivmAadDSGr3FLnYYb6U9RE4-U-SeuImJafTNEJ--4z_En5sm</recordid><startdate>19960601</startdate><enddate>19960601</enddate><creator>Tan, S.V.</creator><creator>Guiloff, R.J.</creator><creator>Henderson, D.C.</creator><creator>Gazzard, B.G.</creator><creator>Miller, R.</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19960601</creationdate><title>Aids-associated vacuolar myelopathy and tumor necrosis factor-alpha (TNFα)</title><author>Tan, S.V. ; Guiloff, R.J. ; Henderson, D.C. ; Gazzard, B.G. ; Miller, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-62e1afe27d7fc0d82236fe3e7cf703e186e35bc5314114c5c870f1fa2cc8b5a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Acquired Immunodeficiency Syndrome - complications</topic><topic>Acquired Immunodeficiency Syndrome - metabolism</topic><topic>Acquired Immunodeficiency Syndrome - pathology</topic><topic>Adult</topic><topic>AIDS</topic><topic>AIDS/HIV</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Cerebrospinal fluid</topic><topic>Cytokines</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>HIV Seronegativity - physiology</topic><topic>HIV Seropositivity - metabolism</topic><topic>HIV1</topic><topic>Humans</topic><topic>Immunodeficiencies</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunohistochemistry</topic><topic>Immunopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Motor Neuron Disease - immunology</topic><topic>Myelin Sheath - pathology</topic><topic>Myelopathy</topic><topic>Paraparesis</topic><topic>Paraparesis, Tropical Spastic - complications</topic><topic>Paraparesis, Tropical Spastic - metabolism</topic><topic>Paraparesis, Tropical Spastic - pathology</topic><topic>Spinal cord disease</topic><topic>Spinal Cord Diseases - complications</topic><topic>Spinal Cord Diseases - metabolism</topic><topic>Spinal Cord Diseases - pathology</topic><topic>TNF</topic><topic>Tumor Necrosis Factor-alpha - analysis</topic><topic>Tumor Necrosis Factor-alpha - cerebrospinal fluid</topic><topic>Vacuoles - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tan, S.V.</creatorcontrib><creatorcontrib>Guiloff, R.J.</creatorcontrib><creatorcontrib>Henderson, D.C.</creatorcontrib><creatorcontrib>Gazzard, B.G.</creatorcontrib><creatorcontrib>Miller, R.</creatorcontrib><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>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the neurological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tan, S.V.</au><au>Guiloff, R.J.</au><au>Henderson, D.C.</au><au>Gazzard, B.G.</au><au>Miller, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aids-associated vacuolar myelopathy and tumor necrosis factor-alpha (TNFα)</atitle><jtitle>Journal of the neurological sciences</jtitle><addtitle>J Neurol Sci</addtitle><date>1996-06-01</date><risdate>1996</risdate><volume>138</volume><issue>1</issue><spage>134</spage><epage>144</epage><pages>134-144</pages><issn>0022-510X</issn><eissn>1878-5883</eissn><coden>JNSCAG</coden><abstract>The spinal cords from 15 patients with AIDS-associated vacuolar myelopathy (VM), 4 AIDS patients without VM, and 5 HIV-seronegative controls, were studied with immunocytochemistry for TNFα. CSF and blood from HIV-seropositive patients with VM ( n = 16), non-vacuolar myelopathies ( n = 8), CNS infection but no clinical myelopathy ( n = 31), no clinical or radiological evidence of CNS disease ( n = 9), and from 7 HIV-seronegative controls with motor neurone disease were assayed for TNFα using an ELISA technique. TNFα was present on immunostaining in all the 15 cords with VM studied. The stained cells were macrophages, microglia and endothelial cells. The amount of immunostaining was higher in cords with VM compared with cords from HIV-seropositive patients without VM ( p = 0.001). The distribution of staining corresponded to the areas of pathology but did not correlate with the severity of the VM. Immunostaining was also higher in the HIV-seropositive group compared to the HIV-seronegative controls ( p = 0.001). There was no significant difference in the levels of TNFα in the CSF of patients with VM compared to any of the other groups studied. Blood levels of TNFα were lower in the HIV-seropositive controls without CNS disease and in the HIV-seronegative MND controls, than in patients with VM, non-vacuolar myelopathies, and CNS disease. CSF TNFα levels did not appear to be a reliable indicator of intramedullary levels. The findings support the hypothesis that TNFα may be relevant in the pathogenesis of vacuolar change in VM.</abstract><cop>Shannon</cop><pub>Elsevier B.V</pub><pmid>8791251</pmid><doi>10.1016/0022-510X(95)00354-5</doi><tpages>11</tpages></addata></record>
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subjects Acquired Immunodeficiency Syndrome - complications
Acquired Immunodeficiency Syndrome - metabolism
Acquired Immunodeficiency Syndrome - pathology
Adult
AIDS
AIDS/HIV
Biological and medical sciences
Case-Control Studies
Cerebrospinal fluid
Cytokines
Enzyme-Linked Immunosorbent Assay
HIV Seronegativity - physiology
HIV Seropositivity - metabolism
HIV1
Humans
Immunodeficiencies
Immunodeficiencies. Immunoglobulinopathies
Immunohistochemistry
Immunopathology
Male
Medical sciences
Middle Aged
Motor Neuron Disease - immunology
Myelin Sheath - pathology
Myelopathy
Paraparesis
Paraparesis, Tropical Spastic - complications
Paraparesis, Tropical Spastic - metabolism
Paraparesis, Tropical Spastic - pathology
Spinal cord disease
Spinal Cord Diseases - complications
Spinal Cord Diseases - metabolism
Spinal Cord Diseases - pathology
TNF
Tumor Necrosis Factor-alpha - analysis
Tumor Necrosis Factor-alpha - cerebrospinal fluid
Vacuoles - pathology
title Aids-associated vacuolar myelopathy and tumor necrosis factor-alpha (TNFα)
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