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dc.contributor.authorKoech, D. K
dc.contributor.authorObel, A. O
dc.contributor.authorMinowada, J
dc.contributor.authorHutchinson, V. A
dc.contributor.authorCummins, J. M
dc.date.accessioned2013-06-11T08:45:27Z
dc.date.available2013-06-11T08:45:27Z
dc.date.issued1990
dc.identifier.citationMol Biother. 1990 Jun;2(2):91-5.en
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/1973045
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/31302
dc.description.abstractThirty eight symptomatic and two asymptomatic patients seropositive for human immunodeficiency virus type-1 (HIV-1) were treated with a natural human interferon alpha (HuIFN alpha). Patients were given 2 IU/kg HuIFN alpha orally once daily in powdered maltose held in the mouth to promote mucosal absorption. This oral immunomodulating HuIFN alpha therapy resulted in an increase in CD4+ lymphocytes, an increase in weight, and a dramatic alleviation of clinical symptoms related to HIV-1 infection.en
dc.language.isoenen
dc.titleLow dose oral alpha-interferon therapy for patients seropositive for human immunodeficiency virus type-1 (HIV-1)en
dc.typeArticleen


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