Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1995-10-10
pubmed:abstractText
Late stages of borrelia Lyme disease infections may be difficult to diagnose because of unspecific symptoms and unreliable laboratory tests, being too unspecific or insensitive. The T cell immune response was thus evaluated in these patients by using a sensitive ELISPOT T cell assay that detects the secretion of IFN-gamma, i.e. a T helper 1 (Th1) response on the single-cell level. Three subcellular fractions of the Lyme borreliosis strain Borrelia afzelii were used for antigenic stimulation. The outer surface protein (Osp) fraction elicited the strongest response, discriminating between borrelia infections (n = 15) compared with other neurological diseases (n = 10) and normal controls (n = 12) (P = 0.0001). The more heterogeneous sonicated borrelia fraction also elicited a strong response, however, also in some of the controls. The flagellin fraction did not have a similar T cell-stimulating effect. When looking at subgroups of borrelia infections, central nervous system (CNS) infections (n = 7) revealed a lower T cell response in blood (P = 0.0128) compared with other borrelia manifestations (n = 8). Cerebrospinal fluid (CSF) lymphocytes were available from three patients with CNS borreliosis, and all showed a compartmentalization with higher responses to the Osp fraction in CSF compared with blood, also in the two patients without any intrathecal-specific antibody synthesis. The ELISPOT method is feasible for detecting a specific IFN-gamma T cell response in borrelia infections. This Th1 response may well be of pathogenic relevance.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-1370170, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-1372558, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-1374425, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-1533765, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-1680337, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-1987874, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-2113474, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-2128520, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-2239139, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-2411827, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-2455606, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-2461134, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-2957307, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-3054554, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-3110648, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-3131436, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-3135295, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-3516878, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-3921611, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-3932581, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-5637478, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-58393, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-7512097, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-7694152, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-7855553, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-8221523, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-8284644, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-8423881, http://linkedlifedata.com/resource/pubmed/commentcorrection/7664493-8460352
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0009-9104
pubmed:author
pubmed:issnType
Print
pubmed:volume
101
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
453-60
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1995
pubmed:articleTitle
The outer surface proteins of Lyme disease borrelia spirochetes stimulate T cells to secrete interferon-gamma (IFN-gamma): diagnostic and pathogenic implications.
pubmed:affiliation
Department of Infections Diseases, Faculty of Health Sciences, University Hospital, Linköping, Sweden.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't