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Original Research

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Immunohistochemical Study of Presence of T Cells, B Cells, and Macrophages in Periradicular Lesions of Primary Teeth

  • Michele Bolan1,*,
  • Daniele de Almeida Lima2
  • Cláudia Pinto Figueiredo3
  • Gabriella Di Giunta2
  • Maria José de Carvalho Rocha1

1Department of Stomatology, Federal University of Santa Catarina

2University Hospital, Federal University of Santa Catarina

3University Hospital, Federal University of Santa Catarina, Vale do Itajaí University

DOI: 10.17796/jcpd.32.4.413p161370186p26 Vol.32,Issue 4,July 2008 pp.287-294

Published: 01 July 2008

*Corresponding Author(s): Michele Bolan E-mail: michelebolan@hotmail.com

Abstract

BACKGROUND: The periapical lesion is the result of a local inflammatory reaction caused by bacteria and its products present on the root canal. The interaction between inflammatory cells and bacteria elicit both specific and non-specific immune responses. OBJETIVE: Due to the lack of studies evaluating the role of the immune system in periapical lesions of primary teeth and considering the potentially systemic effects that these infections can cause in children, especially because of the immaturity of their immune system, we sought to evaluate the presence of T cells, B cells and macrophages on periradicular lesions in primary teeth. STUDY DESIGN: 14 periradicular lesions were analyzed. The immunohistochemistry technique was performed using CD45RO, CD20, CD68 monoclonal antibodies aiming to identify T cells, B cells and macrophages, respectively. Cells were quantified by microscopic analysis of histological sections. RESULTS: Mean percentage of positive cells CD45RO was 11.76; CD20 was 5.25; CD68 was 10.92. Our results showed that T and B cells and macrophages comprise the majority of the inflammatory infiltrate. CONCLUSION: We concluded that both humoral and cell mediated immune reactions take place in periradicular lesions of primary teeth. The immune system plays an important role on the periradicular inflammatory processes in primary teeth.

Keywords

periradicular lesion; immunohistochemistry; B-lymphocytes; T-lymphocytes; macrophages

Cite and Share

Michele Bolan,Daniele de Almeida Lima,Cláudia Pinto Figueiredo,Gabriella Di Giunta,Maria José de Carvalho Rocha. Immunohistochemical Study of Presence of T Cells, B Cells, and Macrophages in Periradicular Lesions of Primary Teeth. Journal of Clinical Pediatric Dentistry. 2008. 32(4);287-294.

References

1. Kaneko T, Okiji T, Kan L, Takagi M, Suda H. Ultrastructural analysis of MHC class II molecule-expressing cells in experimentally induced periapical lesions in rat. J Endod, 27: 337–42, 2001.

2. Susuki T, Kumamoto H, Ooya K, Motegi K. Immunohistochemical analysis of CD1a-labeled Langerhans cells in human dental periapical inflamatory lesions—correlation with inflamatory cells and epithelial cells. Oral Diseases, 7: 336–43, 2001.

3. Cardoso M, Rocha MJC. Identification of factors associated with patho-logical root resorption in traumatized primary teeth. Dent Traumatol. In press.

4. Takahashi K. Microbiological, pathological, inflammatory, immunolog-ical and molecular biological aspects of periradicular disease. Int Endod J, 31: 311–25, 1998.

5. Siqueira JF. and Dantas CJS. Molecular and cellular inflamation mech-anism. Medsi, Rio de Janeiro, p. 238, 2000.

6. Delves PJ, Roitt IM. The Immune System.1. N Engl J Med, 343(1): 37–50, 2000.

7. Delves PJ, Roitt IM. The Immune System.2. N Engl J Med, 343(2): 108–17, 2000.

8. Gorczynski R. and Stanley J. Clinical immunology. Reichmann and Affonso Editors, Rio de Janeiro, p. 355, 2001.

9. Carneiro-Sampaio MMS. and Grumach AS. Pediatric allergy and immunology. 2.ed. Savier, São Paulo, p. 3–27, 1992.

10. Igal LH. and Ron Y. Immunology and inflammation. Basic mechanisms and clinical consequences.McGraw Hill, New York, p. 563–71, 1994.

11. Brook I. Anaerobic infections in children. Adv Pediatr, 47: 395–437, 2000.

12. Stites DP, Terr AI. and Parslow TG. Clinical Immunology. 9.ed. Guan-abara-Koogan, Rio de Janeiro, p. 689, 2000.

13. Serratine ACP. Intensity, localization and consequences of infection in deciduous molar with caries lesions, bone radioluscency in furcation region, floor perforation of pulp chamber: microscopic optic evalua-tion. [Doctoral thesis]. Florianópolis: Faculty of Odontology of Federal University of Santa Catarina; 2002.

14. Bolan M, Rocha MJC. Histopathological study of physiological and pathological resorptions in human primary teeth. Oral Surg Oral Med Oral Pathol, 104: 680–5, 2007.

15. Marton, IJ, Kiss C. Characterization of inflammatory cell infiltrate in dental periapical lesions. Int Endod J, 26(2): 131–6, 1993.

16. Yanagisawa S. Pathologic study of periapical lesions 1. Periapical gran-ulomas: clinical, histopathologic and immunohistopathologic studies. J Oral Pathol, 9: 288–300, 1980.

17. Piattelli A, Artese L, Rosini S, Quaranta M, Musiani P. Immune cells in periapical granuloma: morphological and immunohistochemical char-acterization. J Endod, 17(1): 26–9, 1991.

18. Wallstrom JB, Torabinejad M, Kettering J, Mcmillan P, Linda L. Role of T cells in the pathogenesis of periapical lesions: a preliminary report. Oral Surg Oral Med Oral Pathol, 76(2): 213–8, 1993.

19. Rodini CO, Lara VS. Study of expression of CD68+ macrophages and CD8+ T cells in human granulomas and periapical cysts. Oral Surg Oral Med Oral Pathol, 92: 221–7, 2001.

20. Liapatas S, Nakou M, Rontogianni D. Inflamatory infiltrate of chronic periradicular lesions: na immunohistochemical study. Int Endod J, 36: 464–71, 2003.

21. Philippi CK, Rados PV, Sant’ana Filho M, Barbachan JJD, Quadros OF. Distribuition of CD8 and CD20 lymphocytes in chronic periapical inflammatory lesions. Braz Dent J, 14(3): 182–6, 2003.

22. Rodini CO, Batista AC, Lara VS. Comparative immunohistochemical study of presence of mast cells in apical granulomas and periapical cysts: Possible role of mast cells in the course of human periapical lesions. Oral Surg Oral Med Oral Pathol, 97: 59–63, 2004.

23. Volnei WG, Siqueira WC. Basic histotechnology. 2.ed. Manual, Brasília,

p. 138–44, 1981.

24. Ribeiro FC. Bacterial arrangement in the hard structure of non-vital teeth with necrotic pulp and apical granuloma. [Master thesis]. Bauru: Faculty of Odontology of University of São Paulo; 1982.

25. Alavi AM, Gulabivala K, Speight PM. Quantitative analysis of lympho-cytes and their subsets in periapical lesions. Int Endod J, 31: 233–41, 1998.

26. Torabinejad M, Kettering JD. Identification and relative concentration of B and T lymphocytes in human chronic periapical lesions. J Endod, 11(3): 122–5, 1985.

27. Stashenko P, Yu SM. T helper and T suppressor cell reversal during the development of induced rat periapical lesions. J Dent Res, 68(5): 830–4, 1989.

28. Stashenko P, Yu SM, Wang CY. Kinetics of immune cell and bone resorptive responses to endodontic infections. J Endod, 18(9): 422–6, 1992.

29. Barkhordar RA, Desouza YG. Human T-lymphocyte subpopulations in periapical lesions. Oral Surg Oral Med Oral Pathol, 65(6): 763–6, 1988.

30. Lukic A, Arsenijevic N, Vujanic G, Ramic Z. Quantitative analysis of the immunocompetent cells in periapical granuloma: correlation with the histological characteristics of the lesions. J Endod, 16(3): 119–22, 1990.

31. Kawashima N, Okiji T, Kosaka T, Suda H. Kinetics of macrophages and lymphoid cells during the development of experimentally induced peri-apical lesions in rat molars: a quantitative immunohistochemical study. J Endod, 22(6): 311–6, 1996.

32. Matsuo T, Ebisu S, Shimabukuro Y, Ohtake T, Okada H. Quantitative analysis of immunocompetent cells in human periapical lesions: corre-lations with clinical findings of the involved teeth. J Endod, 18(10): 497–500, 1992.

33. Akamine A, Hashiguchi I, Toriya Y, Maeda K. Immunohistochemical examination on the locatization of macrophages and plasma cells in induced rat periapical lesions. Endod Dent Traumatol, 10: 121–8, 1994.

34. Johannessen AC. Esterase-positive inflammatory cells in human peri-apical lesions. J Endod, 1986; 12(7): 284–8.

35. Angelova A, Takagi Y, Okiji T, Kaneko T, Yamashita Y. Immunocompe-tent cells in the pulp of human deciduous teeth. Arch Oral Biol, 49: 29–36, 2004.

36. Malmstrom M, Natvig JB. IgG rheumatoid factor in dental periapical lesions of patients with rheumatoid disease. Scand J Rheumatol, 4(4): 177–85, 1975.

37. Laine M, Venta I, Hyrkas T, Ma J, Konttinem YT. Chronic inflammation around painless partially erupted third molars. Oral Surg Oral Med Oral Pathol, 95: 277–82, 2003.

38. Radics T, Kiss C, Tar I, Marton IJ. Interleukin-6 and granulocyte-macrophage colony-stimulating factor in apical periodontitis: correla-tion with clinical and histologic findings of the involved teeth. Oral Microbiol Immunol, 18: 9–13, 2003.


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