{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,17]],"date-time":"2026-02-17T23:43:15Z","timestamp":1771371795028,"version":"3.50.1"},"reference-count":131,"publisher":"Oxford University Press (OUP)","issue":"4","license":[{"start":{"date-parts":[[2015,1,20]],"date-time":"2015-01-20T00:00:00Z","timestamp":1421712000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2015,4,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Lyme disease is a multisystem infection transmitted by tick vectors with an incidence of up to 300,000 individuals\/yr in the United States. The primary treatments are oral or i.v. antibiotics. Despite treatment, some individuals do not recover and have prolonged symptoms affecting multiple organs, including the nervous system and connective tissues. Inflammatory arthritis is a common symptom associated with Lyme pathology. In the past decades, \u03b3\u03b4 T cells have emerged as candidates that contribute to the transition from innate to adaptive responses. These cells are also differentially regulated within the synovia of patients affected by RLA. Here, we review and discuss potential cellular mechanisms involving \u03b3\u03b4 T cells and DCs in RLA. TLR signaling and antigen processing and presentation will be the key concepts that we review in aid of understanding the impact of \u03b3\u03b4 T cells in RLA.<\/jats:p>","DOI":"10.1189\/jlb.2ru0714-343rr","type":"journal-article","created":{"date-parts":[[2015,1,21]],"date-time":"2015-01-21T03:47:48Z","timestamp":1421812068000},"page":"653-663","source":"Crossref","is-referenced-by-count":12,"title":["<i>\u03b3\u03b4<\/i> T Cells and dendritic cells in refractory Lyme arthritis"],"prefix":"10.1093","volume":"97","author":[{"given":"Ali","family":"Divan","sequence":"first","affiliation":[{"name":"Texas A&M Health Science , Temple, Texas , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ralph C","family":"Budd","sequence":"additional","affiliation":[{"name":"University of Vermont , Burlington, Vermont , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Richard P","family":"Tobin","sequence":"additional","affiliation":[{"name":"Texas A&M Health Science , Temple, Texas , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M Karen","family":"Newell-Rogers","sequence":"additional","affiliation":[{"name":"Texas A&M Health Science , Temple, Texas , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2015,1,20]]},"reference":[{"key":"2023013012470737900_B1","doi-asserted-by":"crossref","first-page":"1639","DOI":"10.1016\/S0140-6736(03)14798-8","article-title":"Lyme borreliosis","volume":"362","author":"Stanek","year":"2003","journal-title":"Lancet"},{"key":"2023013012470737900_B2","doi-asserted-by":"crossref","first-page":"1089","DOI":"10.1086\/508667","article-title":"The clinical assessment, treatment, and prevention of Lyme disease, human granulocytic anaplasmosis, and babesiosis: clinical practice guidelines by the Infectious Diseases Society of America","volume":"43","author":"Wormser","year":"2006","journal-title":"Clin. 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