Morphological alterations in minor salivary glands of HTLV1+patients: A pilot study

Carregando...
Imagem de Miniatura
Citações na Scopus
0
Tipo de produção
article
Data de publicação
2018
Título da Revista
ISSN da Revista
Título do Volume
Editora
WILEY
Autores
VALE, Daniela Assis do
ANDRADE, Natalia Silva
OLIVEIRA, Augusto Penalva de
BUSSOLOTTI FILHO, Ivo
TRIERVEILER, Marilia
ORTEGA, Karem Lopez
Citação
JOURNAL OF ORAL PATHOLOGY & MEDICINE, v.47, n.10, p.985-990, 2018
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Background Methods Among the complex of HTLV-associated diseases, Sjogren's syndrome (SS) is one of the most controversial. This work aims to detect morphological and inflammatory alterations, including clues of the presence of HTLV-1, in minor salivary glands of patients with dryness symptoms. We have assessed HTLV-1-seropositive patients (HTLV-1 group) and patients with SS (SS group). We used formalin-fixed, paraffin-embedded minor salivary gland tissue to evaluate the morphological aspects and, by means of immunohistochemistry, the presence of Tax protein, CD4, CD8 and CD20 cells. Additionally, viral particles and proviral load were analysed by PCR. Results Conclusion The HTLV-1 group had the highest prevalence of non-specific chronic sialadenitis (85.71%; P = 0.017) and greater amount of T CD8(+) cells. In the SS group, focal lymphocytic sialadenitis (80%; P = 0.017) prevailed, with a greater amount of B CD20(+). Both immunohistochemistry and PCR identified the Tax protein and its gene in the salivary glands of both groups and in similar proportions. The results indicate that HTLV-1-seropositive patients have different patterns of morphological/inflammatory alterations, suggesting a likely difference in the process of immune activation.
Palavras-chave
HTLV-1, immunophenotype, sicca syndrome, Sjogren's syndrome, Tax
Referências
  1. Barbeau B, 2014, RETROVIROLOGY, V11, DOI 10.1186/1742-4690-11-19
  2. Cartier L, 2005, REV MED CHILE, V133, P1183, DOI 10.4067/S0034-98872005001000007
  3. Costa S, 2015, RHEUMATOLOGY, V54, P1056, DOI 10.1093/rheumatology/keu453
  4. Daniels TE, 2011, ARTHRITIS RHEUM-US, V63, P2021, DOI 10.1002/art.30381
  5. DAURIOL L, 1990, NOUV REV FR HEMATOL, V32, P113
  6. do Vale DA, 2017, J ORAL PATHOL MED, V46, P543, DOI 10.1111/jop.12530
  7. EGUCHI K, 1992, ANN RHEUM DIS, V51, P769, DOI 10.1136/ard.51.6.769
  8. Fei C, 2014, J ROY SOC MED, V107, P22, DOI 10.1177/0141076813509981
  9. Futsch N., 2017, VIRUSES, V10
  10. Goncalves DU, 2010, CLIN MICROBIOL REV, V23, P577, DOI 10.1128/CMR.00063-09
  11. Johnsen SJ, 2014, J RHEUMATOL, V41, P2214, DOI 10.3899/jrheum.131527
  12. KAPLAN JE, 1990, J ACQ IMMUN DEF SYND, V3, P1096
  13. MARIETTE X, 1993, ARTHRITIS RHEUM-US, V36, P1423, DOI 10.1002/art.1780361015
  14. Martins FM, 2010, ORAL DIS, V16, P167, DOI 10.1111/j.1601-0825.2009.01638.x
  15. Mizokami A, 1998, SCAND J RHEUMATOL, V27, P435
  16. Nakamura H, 1997, ANN RHEUM DIS, V56, P167, DOI 10.1136/ard.56.3.167
  17. Nakamura H, 2009, RHEUMATOLOGY, V48, P854, DOI 10.1093/rheumatology/kep072
  18. Ohyama Y, 1998, ARTHRITIS RHEUM-US, V41, P1972, DOI 10.1002/1529-0131(199811)41:11<1972::AID-ART12>3.0.CO;2-M
  19. Perzova R, 2013, VIROL J, V10, DOI 10.1186/1743-422X-10-360
  20. POIESZ BJ, 1980, P NATL ACAD SCI-BIOL, V77, P7415, DOI 10.1073/pnas.77.12.7415
  21. POPOVIC M, 1982, NATURE, V300, P63, DOI 10.1038/300063a0
  22. Ramirez E, 2003, VIRUS RES, V91, P231, DOI 10.1016/S0168-1702(02)00276-9
  23. Risselada AP, 2013, SEMIN ARTHRITIS RHEU, V42, P368, DOI 10.1016/j.semarthrit.2012.07.003
  24. Sakai JA, 2001, BLOOD, V98, P1506, DOI 10.1182/blood.V98.5.1506
  25. (SICCA) SsICCA, LAB SAL GLANDS HIST
  26. Tangy F, 1999, J INFECT DIS, V179, P497, DOI 10.1086/314588
  27. TERADA K, 1994, LANCET, V344, P1116, DOI 10.1016/S0140-6736(94)90630-0
  28. Vitali C, 2002, ANN RHEUM DIS, V61, P554, DOI 10.1136/ard.61.6.554