Immunoregulation in onchocerciasis: predominance of Th1‐type responsiveness to low molecular weight antigens of Onchocerca volvulus in exposed individuals without microfilaridermia and clinical disease

Chronic and generalized onchocerciasis is associated with suppression of the parasite‐specific cellular responsiveness, while exposed individuals without parasitological and clinical evidence of infection (endemic normals) display prominent cellular reactivity to Onchocerca volvulus antigens (OvAg). In order to identify those parasite antigens which may account for this differential cellular responsiveness, total adult worm‐derived OvAg were fractionated by means of preparative SDS–PAGE and blot‐elution into 22 antigen fractions of continuously decreasing molecular weight. Peripheral blood mononuclear cells (PBMC) from microfilariae (mf)‐positive onchocerciasis patients (n = 18) proliferated weakly in response to all OvAg fractions. In contrast, in vitro reactivity of PBMC from endemic normals (n = 9) was depressed in response to OvAg of mol. wt 200–30 kD only, while antigens of mol. wt <30 kD induced vigorous proliferation in these individuals compared with the microfilaridermic patients (P < 0.05). Highest proliferative reactivity of cells from endemic normals was observed in response to OvAg of mol. wt 15–11 kD. Furthermore, these low mol. wt antigen fractions induced substantial production of IL‐2 and interferon‐gamma (IFN‐γ) in PBMC from endemic normals, but not in those from onchocerciasis patients. Cells from individuals of both groups secreted similar amounts of IL‐5 in response to all OvAg fractions, with highest production again being induced by low mol. wt OvAg. In contrast, PBMC from onchocerciasis patients clearly produced more IL‐10 than did cells from endemic normals. This augmented IL‐10 production by PBMC from mf‐positive individuals was not only observed after stimulation with OvAg fractions, but was measured in unstimulated control cultures as well. IFN‐γ‐specific mRNA in antigen‐stimulated PBMC from endemic normals appeared to be more prominent than in cells from onchocerciasis patients. However, mRNA transcripts of IL‐10 and IL‐13 were clearly present in patients, but were absent or inconsistently observed in endemic normals. Our results suggest that vigorous Th1‐type cellular responsiveness encountered in endemic normals is restricted to low mol. wt antigens of O. volvulus, while such reactivity will not be present in mf‐positive individuals. Furthermore, spontaneous production of high levels of IL‐10 in onchocerciasis patients is likely to suppress Th1‐type immunity, and thus may favour manifestation of chronic onchocerciasis. These traits of cellular immunity may contribute to the differential outcome of O. volvulus infection, the manifestation of clinical disease, and may also regulate the build up of acquired immunity in humans.

[1]  A. Kelso Th1 and Th2 subsets: paradigms lost? , 1995, Immunology today.

[2]  T. Marti,et al.  Human autoantibody to defensin: disease association with hyperreactive onchocerciasis (sowda) , 1995, The Journal of experimental medicine.

[3]  T. Nutman,et al.  Immunity to onchocerciasis: putative immune persons produce a Th1-like response to Onchocerca volvulus. , 1995, The Journal of infectious diseases.

[4]  E. Ottesen Immune responsiveness and the pathogenesis of human onchocerciasis. , 1995, The Journal of infectious diseases.

[5]  R. Montelaro,et al.  Brugia pahangi: differential granulomatous reactivity of infected jirds (Meriones unguiculatus) to fractions of adult worm extract. , 1995, Experimental parasitology.

[6]  T. Nutman,et al.  Transient changes in cytokine profiles following ivermectin treatment of onchocerciasis. , 1994, The Journal of infectious diseases.

[7]  D. Addiss,et al.  Differential proliferative and interleukin-10 responses to fractionated filarial antigens: preferential recognition by patients with chronic lymphatic dysfunction. , 1994, The Journal of infectious diseases.

[8]  A. Sher,et al.  Interferon-gamma production by peripheral blood mononuclear cells from residents of an area endemic for Schistosoma mansoni. , 1994, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[9]  C. Dreweck,et al.  Ivermectin‐facilitated immunity in onchocerciasis; activation of parasite‐specific Th1‐type responses with subclinical Onchocerca volvulus infection , 1994 .

[10]  M. Stadecker,et al.  Role of IL-10 on antigen-presenting cell function for schistosomal egg-specific monoclonal T helper cell responses in vitro and in vivo. , 1993, Journal of immunology.

[11]  R. Lucius,et al.  Experimental onchocerciasis in chimpanzees: cellular responses and antigen recognition after immunization and challenge with Onchocerca volvulus infective third-stage larvae , 1993, Parasitology.

[12]  T. Nutman,et al.  Regulation of IL-5 in onchocerciasis. A critical role for IL-2. , 1993, Journal of immunology.

[13]  R. Maizels,et al.  T cell responsiveness correlates differentially with antibody isotype levels in clinical and asymptomatic filariasis. , 1993, The Journal of infectious diseases.

[14]  R. Lucius,et al.  Characterization of a recombinant T cell and B cell reactive polypeptide of Onchocerca volvulus. , 1993, Journal of immunology.

[15]  J. Remmé,et al.  Distribution and severity of onchocerciasis in southern Benin, Ghana and Togo. , 1992, Acta tropica.

[16]  C. Dreweck,et al.  Ivermectin‐facilitated immunity in onchocerciasis. Reversal of lymphocytopenia, cellular anergy and deficient cytokine production after single treatment , 1992, Clinical and experimental immunology.

[17]  A. Sher,et al.  IL-10 inhibits parasite killing and nitrogen oxide production by IFN-gamma-activated macrophages. , 1992, Journal of immunology.

[18]  A. Prince,et al.  Identification and characterization of an Onchocerca volvulus cDNA clone encoding a microfilarial surface-associated antigen. , 1992, Molecular and biochemical parasitology.

[19]  A. Sher,et al.  Production of IL-10 by CD4+ T lymphocytes correlates with down-regulation of Th1 cytokine synthesis in helminth infection. , 1991, Journal of immunology.

[20]  T. Nutman,et al.  Immunity to onchocerciasis: recognition of larval antigens by humans putatively immune to Onchocerca volvulus infection. , 1991, The Journal of infectious diseases.

[21]  T. Nutman,et al.  Regulation of the immune response in lymphatic filariasis and onchocerciasis. , 1991, Immunology today.

[22]  S. Kaufmann,et al.  Direct blotting with viable cells of protein mixtures separated by two-dimensional gel electrophoresis. , 1990, Journal of immunological methods.

[23]  F. Perler,et al.  The identification of an Onchocerca-specific recombinant antigen containing a T cell epitope. , 1990, Journal of immunology.

[24]  M. Karam,et al.  Evaluation of a specific enzyme immunoassay for onchocerciasis using a low molecular weight antigen fraction of Onchocerca volvulus. , 1989, The American journal of tropical medicine and hygiene.

[25]  T. Unnasch,et al.  Isolation and characterization of expression cDNA clones encoding antigens of Onchocerca volvulus infective larvae. , 1988, The Journal of clinical investigation.

[26]  J. Ellner,et al.  Cell-mediated immune responses in human infection with Onchocerca volvulus. , 1988, Journal of immunology.

[27]  A. Lujan,et al.  Onchocerciasis and immunity in humans: enhanced T cell responsiveness to parasite antigen in putatively immune individuals. , 1988, The Journal of infectious diseases.

[28]  P. Lammie,et al.  Regulation of jird lymphocyte responsiveness to fractionated antigens of Brugia pahangi. , 1988, Tropical medicine and parasitology : official organ of Deutsche Tropenmedizinische Gesellschaft and of Deutsche Gesellschaft fur Technische Zusammenarbeit.

[29]  T. Nutman,et al.  Brugia malayi antigens associated with lymphocyte activation in filariasis. , 1987, Journal of immunology.

[30]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[31]  J. Ellner,et al.  Non-specific suppression of antigen-induced lymphocyte blastogenesis in Onchocerca volvulus infection in man. , 1983, Clinical and experimental immunology.

[32]  D. Büttner,et al.  Isolation of living adult Onchocerca volvulus from nodules. , 1977, Tropenmedizin und Parasitologie.