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Allergic reactivity and IgG subclasses to a proteinase fraction of Setaria digitata in filariasis

Published online by Cambridge University Press:  05 June 2009

M.K. Beuria
Affiliation:
Parasite Immunology Division, Regional Medical Research Centre (ICMR), Nandankanan Road, Bhubaneswar 751 016, India
M. Bal
Affiliation:
Parasite Immunology Division, Regional Medical Research Centre (ICMR), Nandankanan Road, Bhubaneswar 751 016, India
M.K. Das*
Affiliation:
Parasite Immunology Division, Regional Medical Research Centre (ICMR), Nandankanan Road, Bhubaneswar 751 016, India
*
* Author for correspondence.

Abstract

A low molecular weight fraction (30 KDa) of the cattle filarial parasite Setaria digitata that was earlier demonstrated to have allergenic activity was characterized to be a zinc-dependent cysteine proteinase. Immediate type hypersensitivity (ITH) reaction to the proteinase was evaluated in lymphatic filariasis patients and in endemic controls from Orissa, India. The extent of ITH positivity to the proteinase in infected individuals ranged from 20% in chronic filariasis (CP) patients group to 56% in asymptomatic microfilaraemic carriers (AS). About 62% of endemic normals (EN) were also ITH positive. The serum levels of IgG subclasses were compared in ITH positive and ITH negative filarial patients (AS and CP) as well as in endemic normals (EN) respectively. IgG4 levels were found to be inversely dependent on ITH reaction only in AS groups. Asymptomatic patients (AS) with positive ITH reactivity had lower IgG4 than ITH negative individuals from the same group. The serum levels of other IgG subclasses except IgG2 did not correlate with ITH reactivity. IgG2 levels were higher in ITH negative EN and CP patients but not in the AS group.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 1995

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References

Aalberse, R.C., Van Milligen, F., Tan, K.Y. & Stapel, S.O. (1993) Allergen specific IgG4 in atopic disease. Allergy 48, 559569.Google Scholar
Beauvais, F., Hieblot, C., Burtin, C. & Benveniste, J. (1990) Bimodal IgG4 mediated human basophil activation: role of eosinophils. Journal of Immunology 14, 38813890.Google Scholar
Beuria, M.K. & Das, M.K. (1992) Immune responses to an allergenic fraction of Setaria digitata in human filariasis. Journal of Bioscience 17, 453461.CrossRefGoogle Scholar
Chappel, C.L., Kalter, D.C. & Dresden, M.H. (1988) The hypersensitivity response to the adult worm proteinase SMW 32 in Schistosoma mansoni in infected mice. American Journal of Tropical Medicine and Hygiene 39, 463468.CrossRefGoogle Scholar
Chua, K.Y., Stewart, G.A., Thomas, W.R., Simpson, R.J., Dilworth, R.J., Plozza, T.M. & Turner, K.J. (1988) Sequence analysis of cDNA coding for a major house dust allergen, Der p 1:homology with cysteine proteases. Journal of Experimental Medicine 167, 174182.CrossRefGoogle Scholar
Das, M.K., Beuria, M.K. & Dash, A.P. (1992) Immunoglobulin E and G4 antibodies to infective larvae in a Wuchereria bancrofti endemic population. International Archives of Allergy and Immunology 99, 118122.CrossRefGoogle Scholar
Del Giudice, G., Engers, S.D., Tougene, C., Bitto, S., Weiss, N., Verdini, A.S., Pressi, A., Degremont, A., Frey Vogel, T.A., Lambert, P.H. & Tanner, M. (1987) Antibodies to the repetitive epitope of Plasmodium falciparum circumsporozoite protein in a rural Tanzanian community: a longitudinal study of 132 children. American Journal of Tropical Medicine and Hygiene 36, 203212.CrossRefGoogle Scholar
Finkelman, F.D. & Urban, J.F. Jr (1992) Cytokines: making the right choice. Parasitology Today 8, 311314.Google Scholar
Godfrey, R.C. & Gradidge, C.F. (1976) Allergic sensitization of human lung fragments prevented by saturation of IgE binding sites. Nature 259, 484486.CrossRefGoogle ScholarPubMed
Hagel, I., Lynch, N.R., Perez, M.DiPrisco, M.C., Lopez, R. & Rojas, E. (1993) Modulation of the allergic reactivity of slum children by helminthic infection. Parasite Immunology 15, 311315.Google Scholar
Hussain, R., Hamilton, R.G., Kumarswami, V., Adkinson, N.F. Jr. & Ottesen, E.A. (1981) IgE responses in human filariasis I. Quantitation of filaria-specific IgE. Journal of Immunology 127, 16231628.Google Scholar
Hussain, R., Groge, M. & Ottesen, E.A. (1987) IgG antibody subclasses in human filariasis. Differential recognition of parasite antigens correlates with different clinical manifestation of infection.Journal of Immunology 138,27942798.CrossRefGoogle Scholar
Hussain, R., Poindexter, R.W. & Ottesen, E.A. (1992) Control of allergic reactivity in human filariasis. Predominant localisation of blocking antibody to the IgG4 subclass. Journal of Immunology 148, 27312737.CrossRefGoogle Scholar
Jimeno, J., Lombardero, M.Carrerira, J. & Moscoso Del Pardo, J. (1992) Presence of IgC4 on the membrane of human basophils. Histamine release in induced by monoclonal antibodies directed against Fab but not the Fc region of the IgG4 molecule. Clinical and Experimental Allergy 22, 10071014.CrossRefGoogle Scholar
Knox, D.P. & Kennedy, M.W. (1988) Proteinases released by the parasitic larvae stages of Ascaris suum and their inhibition by antibody. Molecular and Biochemical Parasitology 28, 207216.CrossRefGoogle ScholarPubMed
Kwan-lim, G.E., Forsyth, K.P. & Maizels, R.M. (1990) Filaria specific IgG4 response correlates with active Wuchereria bancrofti infection. Journal of Immunology 145, 42984305.CrossRefGoogle Scholar
Lichtenstein, L.M., Holtzman, N.A. & Brunetle, L.S. (1968) A quantitative in vitro study of the chromatographic distribution and immunoglobulin characteristics of human blocking antibody. Journal of Immunology 101, 317324.Google Scholar
McKerrow, J.H., Sun, E., Rosenthal, P.J. & Bouvier, J. (1993) The proteases and pathogenicity of parasitic protozoa. Annual Reviews of Microbiology 47, 821853.Google Scholar
Nawata, Y., Koike, T. & Tautsumi, A. (1988) Anti-IgE antibody in patients with parasite infection. Japanese Journal of Allergy 37, 204.Google Scholar
Oglivie, B. (1964) Reagin-like antibodies in animals immune to helminth parasites. Nature 204, 9192.CrossRefGoogle Scholar
Parish, W.E. (1974) Skin sensitizing non-IgE antibodies. Association between human IgG S-TS and IgG4 pp. 1928in Brent, L. & Holborow, J. (Eds) Progress in Immunology II Part 4. North Holland.Google Scholar
Pritchard, D.I. (1993) Immunity to helminths: is too much IgE parasite-rather than host protective? Parasite Immunology 15 59.CrossRefGoogle ScholarPubMed
Senfit, A.W. & Maddinson, S.E. (1975) Hypersensitivity to parasite proteolytic enzyme in schistosomiasis. American Journal of Tropical Medicine and Hygiene 24, 8389.Google Scholar
Shakib, F. & Powell-Richards, A. (1991) Elucidation of the epitope localisation of human auto anti-IgE: recognition of two epitopes located within the CE2 and CE4 domains. International Archives of Allergy and Applied Immunology 95, 102108.CrossRefGoogle Scholar
Stanworth, D.R. & Smith, A.K. (1973) Inhibition of reaginmediated PCA reaction in baboons by the human IgG4 subclass. Clinical Allergy 3, 3741.Google Scholar
Yamauchi, N., Ito, K., Suko, M., Ishii, A. & Miyamoto, T. (1986) IgG2 antibodies block IgE antibody-induced asthma in guinea pigs. International Archives of Allergy and Applied Immunology 80, 7680.CrossRefGoogle ScholarPubMed