Lymphocyte proliferation and cytokine production in mice infected with different geographical isolates of Trichinella spiralis

Antigen‐specific proliferative responses and cytokine production were measured in lymphocytes taken from inbred NIH mice infected with different isolates of Trichinella spiralis. Stimulation with muscle larval homogenate antigen produced high proliferative responses, cells responding more strongly to antigen from one isolate (London‐L) than to antigens of the other two isolates (Spanish‐S and Polish‐P). Antigen from the P‐isolate elicited relatively poor responses. There was considerable, although variable, cross reactivity between isolate antigens and this was reflected in proliferation to heterologous stimulation. When pulsed with the mitogen Concanavalin A (Con‐A) mesenteric lymph node cells (MLNC) produced IFN‐gamma on day four post infection but not on day eight. In contrast, production of IL‐4 and IL‐5 was greatest on day eight. Differences were seen in levels of cytokine production between cells taken from mice infected with different isolates. These data show a sequential activation of Th1 and Th2 cells during infection with T. spiralis isolates, and suggest that the level of activation of each Th subset is influenced by the antigenic characteristics of each isolate.

[1]  K. Else,et al.  Correlations between worm burden and markers of Th1 and Th2 cell subset induction in an inbred strain of mouse infected with Trichuris muris , 1993, Parasite immunology.

[2]  D. Wakelin,et al.  Vaccination against Trichinella spiralis in mice using antigens from different isolates , 1993, Parasitology.

[3]  D. Wakelin,et al.  Influence of variation in host strain and parasite isolate on inflammatory and antibody responses to Trichinella spiralis in mice , 1993, Parasitology.

[4]  K. Else,et al.  Genetic influences upon eosinophilia and resistance in mice infected with Trichinella spiralis , 1992, Parasitology.

[5]  C. Hayes,et al.  Influence of resistant and susceptible genotype, IL-1, and lymphoid organ on Trichinella spiralis-induced cytokine secretion. , 1992, Journal of immunology.

[6]  F. Liew,et al.  Thymopentin reduces the susceptibility of aged mice to cutaneous leishmaniasis by modulating CD4 T-cell subsets. , 1992, Immunology.

[7]  K. Else,et al.  Modulation of cytokine production and response phenotypes in murine trichuriasis , 1992, Parasite immunology.

[8]  K. Else,et al.  Cellular immune responses to the murine nematode parasite Trichuris muris. II. Differential induction of TH-cell subsets in resistant versus susceptible mice. , 1992, Immunology.

[9]  K. Else,et al.  Helper T-cell subsets in mouse trichuriasis. , 1991, Parasitology today.

[10]  K. Else,et al.  Host protective immunity to Trichinella spiralis in mice: activation of Th cell subsets and lymphokine secretion in mice expressing different response phenotypes. , 1991, Immunology.

[11]  E. A. Kelly,et al.  IFN-gamma- and IL-5-producing cells compartmentalize to different lymphoid organs in Trichinella spiralis-infected mice. , 1991, Journal of immunology.

[12]  K. Else,et al.  Cellular immune responses to the murine nematode parasite Trichuris muris. I. Differential cytokine production during acute or chronic infection. , 1991, Immunology.

[13]  R. Locksley,et al.  Helper T-cell subsets in mouse leishmaniasis: induction, expansion and effector function. , 1991, Immunology today.

[14]  T. Mosmann,et al.  The role of IL-10 in crossregulation of TH1 and TH2 responses. , 1991, Immunology today.

[15]  K. HayGlass,et al.  Anti-interferon gamma treatment blocks the ability of glutaraldehyde- polymerized allergens to inhibit specific IgE responses , 1991, The Journal of experimental medicine.

[16]  T. Mosmann,et al.  Interleukin 10: a novel stimulatory factor for mast cells and their progenitors , 1991, The Journal of experimental medicine.

[17]  A. Sher,et al.  Downregulation of Th1 cytokine production accompanies induction of Th2 responses by a parasitic helminth, Schistosoma mansoni , 1991, The Journal of experimental medicine.

[18]  F. Liew,et al.  A repetitive peptide of Leishmania can activate T helper type 2 cells and enhance disease progression , 1990, The Journal of experimental medicine.

[19]  C. Hayes,et al.  Evidence for differential induction of helper T cell subsets during Trichinella spiralis infection. , 1989, Journal of immunology.

[20]  J. Langhorne,et al.  Frequencies of CD4+ T cells reactive with Plasmodium chabaudi chabaudi: distinct response kinetics for cells with Th1 and Th2 characteristics during infection. , 1989, International immunology.

[21]  R. Bell,et al.  IL-2 production, IL-2 receptor expression, and IL-2 responsiveness of spleen and mesenteric lymph node cells from inbred mice infected with Trichinella spiralis. , 1989, Journal of immunology.

[22]  T. Roach,et al.  Host predisposition to trichuriasis: the mouse — T. muris model , 1989, Parasitology.

[23]  K. Else,et al.  Genetic variation in the humoral immune responses of mice to the nematode Trichuris muris , 1989, Parasite immunology.

[24]  K. Else,et al.  The effects of H-2 and non-H-2 genes on the expulsion of the nematode Trichuris muris from inbred and congenic mice , 1988, Parasitology.

[25]  T. Dick,et al.  Trichinella spiralis infections of inbred mice: immunologically specific responses induced by different Trichinella isolates. , 1988, The Journal of parasitology.

[26]  C. Sanderson,et al.  Molecular and Cellular Biology of Eosinophil Differentiation Factor (Interleukin‐5) and its Effects on Human and Mouse B Cells , 1988, Immunological reviews.

[27]  W. Paul,et al.  Interferon-gamma and B cell stimulatory factor-1 reciprocally regulate Ig isotype production. , 1987, Science.

[28]  R. Coffman,et al.  A T cell activity that enhances polyclonal IgE production and its inhibition by interferon-gamma. , 1986, Journal of immunology.

[29]  R. Grencis,et al.  L3T4-positive T lymphoblasts are responsible for transfer of immunity to Trichinella spiralis in mice. , 1985, Immunology.

[30]  D. Wakelin,et al.  Cortisone-induced immunotolerance to nematode infection in CBA/Ca mice. II. A model for human chronic trichuriasis. , 1983, Immunology.

[31]  D. Wakelin,et al.  Genetic control of immunity to Trichinella spiralis: influence of H-2-linked genes on immunity to the intestinal phase of infection. , 1983, Immunology.

[32]  D. Wakelin,et al.  Genetic factors controlling the intestinal mast cell response in mice infected with Trichinella spiralis. , 1982, Clinical and experimental immunology.

[33]  R. Grencis,et al.  Short lived, dividing cells mediate adoptive transfer of immunity to Trichinella spiralis in mice. II. In vivo characteristics of the cells. , 1982, Immunology.

[34]  R. Grencis,et al.  Specific cross-immunity between Trichinella spiralis and Trichuris muris: immunization with heterologous infections and antigens and transfer of immunity with heterologous immune mesenteric lymph node cells , 1982, Parasitology.

[35]  F. Leenstra,et al.  Trichinella spiralis infection in congenitally athymic (nude) mice. Parasitological, serological and haematological studies with observations on intestinal pathology. , 1977, Immunology.

[36]  D. Wakelin,et al.  Immunological interactions between Trichinella spiralis and Trichuris muris in the intestine of the mouse , 1977, Parasitology.

[37]  D. Wakelin,et al.  Immunity to primary and challenge infections of Trichinella spiralis in mice: a re-examination of conventional parameters , 1976, Parasitology.

[38]  D. Wakelin Acquired immunity to Trichuris muris in the albino laboratory mouse , 1967, Parasitology.

[39]  P. Openshaw,et al.  Distinct patterns of T- and B-cell immunity to respiratory syncytial virus induced by individual viral proteins. , 1993, Vaccine.

[40]  M. Clerici,et al.  A TH1-->TH2 switch is a critical step in the etiology of HIV infection. , 1993, Immunology today.

[41]  R. Coffman,et al.  Regulation of immunity to parasites by T cells and T cell-derived cytokines. , 1992, Annual review of immunology.

[42]  R. Coffman,et al.  TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties. , 1989, Annual review of immunology.

[43]  E. Puré,et al.  T CELL-DERIVED B CELL DIFFERENTIATION FACTORS: (BCDF) : DEFINITION OF BCDFμ AND BCDFγ , 1982 .