ArticleClinical and diagnostic laboratory immunology1996
Immunological characterization of a recombinant 27-kilodalton antigenic protein from Paracoccidioides brasiliensis.
Article in Clinical and diagnostic laboratory immunology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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Who cites it
7 citing papers in PubMed, 27 citations in OpenAlex.
- Additive effect of rPb27 immunization and chemotherapy in experimental paracoccidioidomycosis.PloS one · 2011Article
- Evidence for positive selection in putative virulence factors within the Paracoccidioides brasiliensis species complex.PLoS neglected tropical diseases · 2008Article
- Expression of antibodies directed to Paracoccidioides brasiliensis glycosphingolipids during the course of paracoccidioidomycosis treatment.Clinical and vaccine immunology : CVI · 2007Article
- Combined use of Paracoccidioides brasiliensis recombinant 27-kilodalton and purified 87-kilodalton antigens in an enzyme-linked immunosorbent assay for serodiagnosis of paracoccidioidomycosis.Journal of clinical microbiology · 2003Article
- Current status of nonculture methods for diagnosis of invasive fungal infections.Clinical microbiology reviews · 2002Review
- Use of the 27-kilodalton recombinant protein from Paracoccidioides brasiliensis in serodiagnosis of paracoccidioidomycosis.Clinical and diagnostic laboratory immunology · 1998Article
- Identification and purification of specific Penicillium marneffei antigens and their recognition by human immune sera.Journal of clinical microbiology · 1998Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We report the expression in Escherichia coli of a 27-kDa antigenic protein from Paracoccidioides brasiliensis. When analyzed by immunoblotting, this recombinant antigenic protein was recognized by antibodies present in the sera of 40 of the 44 paracoccidioidomycosis patients studied. No cross-reactions were observed with sera from patients with other mycoses (histoplasmosis, aspergillosis, cryptococcosis, sporotrichosis, and chromoblastomycosis) or with tuberculosis.
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Registered trials
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