Effect of pre-immunization by killed Mycobacterium bovis and vaccae on immunoglobulin E response in ovalbumin-sensitized newborn mice

Pediatric Allergy and Immunology

Volumn 10, Issue 2, 1999, Pages 107-111

  Tükenmez, Faruk ^a   Bahçeciler, Nerin Nadir ^a   Barlan, Işil Berat ^a,b   Başaran, Müjdat Mustafa ^a  

^a MARMARA UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

^b Kantarci Riza Sok   (Turkey)

Author keywords

Atopy; Balb; c mice; IgE; Mycobacterium vaccae; Newborn

Indexed keywords

BACTERIAL VACCINE; IMMUNOGLOBULIN E; OVALBUMIN; ANTIALLERGIC AGENT; INACTIVATED VACCINE;

ANIMAL EXPERIMENT; ANTIBODY RESPONSE; ARTICLE; COLONY FORMING UNIT; CONTROLLED STUDY; FEMALE; IMMUNIZATION; INTRAPERITONEAL DRUG ADMINISTRATION; MALE; MOUSE; MYCOBACTERIUM BOVIS; MYCOBACTERIUM VACCAE; NEWBORN; NONHUMAN; PRIORITY JOURNAL; ALLERGY; ANIMAL MODEL; CELLULAR IMMUNITY; IMMUNOGLOBULIN BLOOD LEVEL; LYMPHOCYTE DIFFERENTIATION; PROVOCATION TEST; RISK REDUCTION; TH1 CELL; TH2 CELL;

ANIMALS; BACTERIAL VACCINES; FEMALE; HYPERSENSITIVITY; IMMUNIZATION; IMMUNOGLOBULIN E; MALE; MICE; MICE, INBRED BALB C; MYCOBACTERIUM; MYCOBACTERIUM BOVIS; OVALBUMIN; PREGNANCY; STATISTICS, NONPARAMETRIC; VACCINES, INACTIVATED;

EID: 17944398846     PISSN: 09056157     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-3038.1999.00029.x     Document Type: Article

References (29)

1. MOSMANN TR, CHERWINSKI H, BOND MW, GIEDLIN MA, COFFMAN RL. Two types of murine helper T cell colone. I. Definition according to profiles of lymphokine activities and secreted proteins. J Immonol 1986: 136: 2348-57.
2. ABBAS AK, MURPHY KM, SHER A. Functional diversity of helper T lymphocytes. Nature 1996: 383: 787-793.
3. CARRER LL, DUTTON RW. Type 1 and type 2: a fundamental dichotomy for all T-cell subsets? Curr Opin Immunol 1996: 8: 336-42.
4. SHER A, GAZZINELLI RT, OSWALD LP, et al. Role of T cell derived cytokines in the downregulation of immune responses in parasitic and retroviral infection. Immunol Rev 1992: 127: 183-204.
5. ROMAGNANI S. Induction of Th1 and Th2 responses: a key role for the 'natural' immune response? Immunol Today 1992: 13: 379-81.
6. WEIZMAN M, GORTMAKER SL, SOBOL AM, PERRIN JM. Recent trends in the prevalence and severity of childhood asthma. JAMA 1992: 268: 2673-7.
7. ANDRAE S, AXELSON O, BJÖRKSTEN B, FREDRIKSSON M, KJELLMAN N-IM. Symptoms of bronchial hyperactivity and asthma in relation to environmental factors. Arch Dis Child 1988: 63: 473-8.
8. STRACHAN DP. Damp housing and childhood asthma: validation of reporting of symptoms. BMJ 1988: 297: 1223-6.
9. ISHIZAKI T, KOIZUMI K, IKEMORI R, ISHIAMA Y, KUSHIBIKI E. Studies of prevalence of Japanese cedar pollinosis among the residents in a densely cultivated area. Ann Allergy 1987: 58: 265-70.
10. WICKMAN M, NORDVALL SL, PERSHAGEN G. Risk factors in early childhood for sensitization to airborne alergens. Pediatr Allergy Immunol 1992: 3: 128-33.
11. WEGMAN TG, LIN H, GILBERT L, MOSMANN TR. Bidirectional cytokine interactions in the maternal-fetal relationship: is successful pregnancy a Th2 phenomenon? Immunol Today 1993: 14: 353-56.
12. ROMAGNANI S. Regulation of the development of type-2 T helper cells in allergy. Curr Opin Immunol 1994: 6: 838-46.
13. MOSMANN TR, SAD S. The expanding universe of T-cell subsets. Th1, Th2 and more. Immunol Today 1996: 17: 138-46.
14. DEL PRETE GF, CARLI MD, MASTOMAURO C, et al. Purified protein derivative of mycobacteria tuberculosis and excretory-secretory antigen(s) of Toxocara canis expand in vitro human T cells with stable and opposite (Type 1 T helper or type 2 T helper) profile of cytokine production. J Clin Invest 1991: 88: 346-50.
15. SHIRAKAWA T, ENOMTO T, SHIMAZU S, HOPKIN JM. The inverse association between tuberculin responses and atopic disorder. Science 1997: 275: 77-9.
16. ERB KJ, HOLLOWAY JW, SOBECK A, MOLL H, GROS G. Infection of mice with Mycobacterium bovis-Bacillus Calmette Guerin-(BCG) suppresses allergen induced airway eosinophilia. J Exp Med 1998: 187: 561-9.
17. WANG CC, ROOK Gaw. Inhibition of an established allergic response to ovalbumin in BALB/c mice by killed mycobacterium vaccae. Immunology 1998: 93: 307-13.
18. SKINNER MA, YUAN S, PRESTIDGE R, CHUK D, WATSON JD, TAN PL. Immunization with heat killed Mycobacterium vaccae stimulates CD8+ cytotoxic T cells specific for macrophage infected with mycobacterium tuberculosis. Infect Immun 1997: 65: 4525-30.
19. STANFORD JL, STANFORD CA. Immunotherapy of tuberculosis with mycobacterium vaccae NCTC 11659. Immunobiology 1994: 191: 555-63.
20. HERNANDEZ PR, PAVÖN LARR, ARRIAGA K, et al. Pathogenesis of tuberculosis in mice exposed to low and high doses of an environmental mycobacterial saprophyte before infection. Infect Immun 1997: 65: 3317-27.
21. TSICOPOULUS A, HAMID Q. Preferential rnRNA expression of Th1 type cells in classical delayed type hypersensitivity reaction in human skin. J Immunol 1992: 148: 2058.
22. MAGGI E, PARRNCHI P. Reciprocal regulatory effects of IFN gamma and IL-4 on the in vitro development of human Th1 and Th2 clones. J Immunol 1992: 148: 2142.
23. HUYGEN K, LOZES E, GILES B, et al. Mapping of Th1 helper T cell epitopes on major secreted mycobacterial antigen 85A in mice infected with live Mycobacterium bovis BCG. Infect Immun 1994: 62: 363-370.
24. LIN AY, ZHU SZ. 301 cases of bronchial asthma treated by kahusu. Chin J Integ Trad West Med 1991: 11: 209-11.
25. STRANNEGARD IL, LARSON LO, WENNERGEN G, STRANNEGRAD O. Prevalence of allergy in children relation to prior BCG vaccination and infection with atypical mycobacteria. Allergy 1998: 53: 249-54.
26. STANFORD JL, ROOK GAW, BAHR GM, et al. Mycobacterium vaccae in immunoprophylaxis and immunotherapy of leprosy and tuberculosis. Vaccine 1990: 8: 525-30.
27. SKINNER M, YUAN S, PRESTIDGE R, WATSON JD, TAN PLJ. Heat killed Mycobacterium vaccae as an adjuvant and vaccine for tuberculosis. Stimulation of CD8+ cytotoxic T cells. Vaccine Weekly 1997: 6: 23.
28. BAKIR M, TÜKENMEZ F, GÜREL A, et al. Heat killed BCG decreased serum IgE level in ovalbumin sensitized mice. J Allergy Clin Immunol 1997: 99: 1770.
29. RENZ H, SMITH HR, HENSON JE, et al. Aerosolized antigen exposure without adjuvant causes increased IgE production and increased airway responsiveness in the mouse. J Allergy Clin Immunol 1992: 89: 1127-38.