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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
|
pubmed:dateCreated |
1979-3-24
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pubmed:abstractText |
Six of 17 pemphigus patients (35%) treated during a six-year period with immunosuppressive agents and/or corticosteroids have had prolonged clinical and immunologic remissions off all therapy. All were treated until serum and tissue bound pemphigus antibodies could no longer be detected. The length of remission has ranged from 1 1/2 years to 4 years. Three of these six patients relapsed after being clinically and serologically free of pemphigus for 19, 20, and 48 months. Seven additional patients are clinically free of disease with insignificant pemphigus antibody titers of 10 or less. Therapy now is being discontinued gradually in these patients. This preliminary study demonstrates that (1) a large percentage of pemphigus patients may have a prolonged clinical and immunological remission after successful therapy; (2) maintenance therapy may not be required to preserve the remission; (3) monitoring serum and in vivo bound pemphigus antibody is of value in regulating therapy in pemphigus patients.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0003-987X
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
114
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1769-72
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pubmed:dateRevised |
2008-3-17
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pubmed:meshHeading |
pubmed-meshheading:736583-Adrenal Cortex Hormones,
pubmed-meshheading:736583-Adult,
pubmed-meshheading:736583-Antibodies,
pubmed-meshheading:736583-Humans,
pubmed-meshheading:736583-Immunosuppressive Agents,
pubmed-meshheading:736583-Male,
pubmed-meshheading:736583-Middle Aged,
pubmed-meshheading:736583-Pemphigus,
pubmed-meshheading:736583-Remission, Spontaneous
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pubmed:year |
1978
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pubmed:articleTitle |
Fate of pemphigus antibody following successful therapy. Preliminary evaluation of pemphigus antibody determinations to regulate therapy.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
|