Improved detection of Pneumocystis carinii by an immunofluorescence technique using monoclonal antibodies.

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Improved detection of Pneumocystis carinii by an immunofluorescence technique using monoclonal antibodies. / Orholm, M; Holten-Andersen, W; Lundgren, Jens Dilling.

I: European Journal of Clinical Microbiology & Infectious Diseases, Bind 9, Nr. 12, 1990, s. 880-885.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskning

Harvard

Orholm, M, Holten-Andersen, W & Lundgren, JD 1990, 'Improved detection of Pneumocystis carinii by an immunofluorescence technique using monoclonal antibodies.', European Journal of Clinical Microbiology & Infectious Diseases, bind 9, nr. 12, s. 880-885. <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=2073898&query_hl=39>

APA

Orholm, M., Holten-Andersen, W., & Lundgren, J. D. (1990). Improved detection of Pneumocystis carinii by an immunofluorescence technique using monoclonal antibodies. European Journal of Clinical Microbiology & Infectious Diseases, 9(12), 880-885. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=2073898&query_hl=39

Vancouver

Orholm M, Holten-Andersen W, Lundgren JD. Improved detection of Pneumocystis carinii by an immunofluorescence technique using monoclonal antibodies. European Journal of Clinical Microbiology & Infectious Diseases. 1990;9(12):880-885.

Author

Orholm, M ; Holten-Andersen, W ; Lundgren, Jens Dilling. / Improved detection of Pneumocystis carinii by an immunofluorescence technique using monoclonal antibodies. I: European Journal of Clinical Microbiology & Infectious Diseases. 1990 ; Bind 9, Nr. 12. s. 880-885.

Bibtex

@article{74386607dddb4e62bd5faeed37e47e7b,
title = "Improved detection of Pneumocystis carinii by an immunofluorescence technique using monoclonal antibodies.",
abstract = "To assess whether a recently developed indirect immunofluorescent stain using monoclonal antibodies was more sensitive in detecting Pneumocystis carinii than the combination of Giemsa and methenamine silver nitrate stains which has routinely been used in the laboratory, 88 lavage fluid specimens and 34 induced sputum specimens were examined. All specimens were stained by five techniques: immunofluorescence using a combination of three monoclonal antibodies (from the National Institutes of Health, USA), immunofluorescence using a single monoclonal antibody (from Dakopatts), Giemsa, methenamine silver nitrate and toluidine blue O. Immunofluorescence using the monoclonal antibodies from the NIH was significantly more sensitive than any other single staining method and than the combination of Giemsa and methenamine silver nitrate staining. The study also showed that the cytospin centrifuge was very suitable for the preparation of slides with lavage fluid and processed induced sputum. Finally, the sensitivity of examination of induced sputum to detect Pneumocystis carinii was found to be 50% when compared with bronchoalveolar lavage fluid. However, this sensitivity may increase through practice.",
author = "M Orholm and W Holten-Andersen and Lundgren, {Jens Dilling}",
year = "1990",
language = "English",
volume = "9",
pages = "880--885",
journal = "European Journal of Clinical Microbiology & Infectious Diseases",
issn = "0934-9723",
publisher = "Springer",
number = "12",

}

RIS

TY - JOUR

T1 - Improved detection of Pneumocystis carinii by an immunofluorescence technique using monoclonal antibodies.

AU - Orholm, M

AU - Holten-Andersen, W

AU - Lundgren, Jens Dilling

PY - 1990

Y1 - 1990

N2 - To assess whether a recently developed indirect immunofluorescent stain using monoclonal antibodies was more sensitive in detecting Pneumocystis carinii than the combination of Giemsa and methenamine silver nitrate stains which has routinely been used in the laboratory, 88 lavage fluid specimens and 34 induced sputum specimens were examined. All specimens were stained by five techniques: immunofluorescence using a combination of three monoclonal antibodies (from the National Institutes of Health, USA), immunofluorescence using a single monoclonal antibody (from Dakopatts), Giemsa, methenamine silver nitrate and toluidine blue O. Immunofluorescence using the monoclonal antibodies from the NIH was significantly more sensitive than any other single staining method and than the combination of Giemsa and methenamine silver nitrate staining. The study also showed that the cytospin centrifuge was very suitable for the preparation of slides with lavage fluid and processed induced sputum. Finally, the sensitivity of examination of induced sputum to detect Pneumocystis carinii was found to be 50% when compared with bronchoalveolar lavage fluid. However, this sensitivity may increase through practice.

AB - To assess whether a recently developed indirect immunofluorescent stain using monoclonal antibodies was more sensitive in detecting Pneumocystis carinii than the combination of Giemsa and methenamine silver nitrate stains which has routinely been used in the laboratory, 88 lavage fluid specimens and 34 induced sputum specimens were examined. All specimens were stained by five techniques: immunofluorescence using a combination of three monoclonal antibodies (from the National Institutes of Health, USA), immunofluorescence using a single monoclonal antibody (from Dakopatts), Giemsa, methenamine silver nitrate and toluidine blue O. Immunofluorescence using the monoclonal antibodies from the NIH was significantly more sensitive than any other single staining method and than the combination of Giemsa and methenamine silver nitrate staining. The study also showed that the cytospin centrifuge was very suitable for the preparation of slides with lavage fluid and processed induced sputum. Finally, the sensitivity of examination of induced sputum to detect Pneumocystis carinii was found to be 50% when compared with bronchoalveolar lavage fluid. However, this sensitivity may increase through practice.

M3 - Journal article

VL - 9

SP - 880

EP - 885

JO - European Journal of Clinical Microbiology & Infectious Diseases

JF - European Journal of Clinical Microbiology & Infectious Diseases

SN - 0934-9723

IS - 12

ER -

ID: 40213351