RESUMEN
Superoxide plays a crucial role in innate immunity to various pathogens. We examined the role of superoxides in the transmission of malaria using gp91phox knockout (X-CGD) mice that lack the ability to produce superoxide. Mosquitoes that fed on X-CGD mice infected intraperitoneally with Plasmodium berghei NK65 ANKA formed more oocysts than did those that fed on control mice at any day after infection. The number of oocysts peaked on day 5 post-infection in X-CGD and control mice and then decreased significantly after day 5 post-infection. However, on day 7 post-infection, the infectivity of gametocytes in X-CGD mice was significantly higher than that in control mice. These results show that two pathways, superoxide-dependent and -independent, are involved in the host systems regulating the transmission of malaria and inhibiting gametocyte development.
Asunto(s)
Malaria/prevención & control , Malaria/transmisión , NADPH Oxidasas , Plasmodium berghei/patogenicidad , Superóxidos/metabolismo , Animales , Anopheles/parasitología , Glicoproteínas de Membrana/genética , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , NADPH Oxidasa 2 , Recuento de Huevos de Parásitos , Plasmodium berghei/crecimiento & desarrolloRESUMEN
Mosquito bites can elicit dermal hypersensitivity reactions, but little is known about the chemotactic factors for host leukocytes in mosquito saliva. In this study, we determined that saliva from a malarial vector mosquito, Anopheles stephensi, possesses intense neutrophil chemotactic activity. In contrast, the midgut extract had only marginal neutrophil chemotactic activity. Eosinophil chemotactic activity was detected in the midgut but not in the saliva. According to the results of size-exclusion HPLC on a G3000SW column and Western blot analysis, the apparent molecular weight (MW) of the main neutrophil chemotactic factor (NCF) was estimated to be 200 kDa. NCF could bind with IgG from the pooled serum of Solomon islanders, whereas not with that of healthy Japanese. NCF activity was increased upon heating to 56 degrees C for 30 min or protease digestion, whereas it was affected by periodate treatment. Protease-digested NCF and naive NCF bound to lentil lectin-Sepharose, and both were eluted with a competitive sugar, methyl-alpha-D-glucoside. These results indicate that A. stephensi saliva-derived NCF is a high MW glycoprotein, and its protein moiety is important for neutrophil chemotactic activity. This NCF is thought to contribute to the inflammatory reactions through the accumulation of neutrophils at the site of the mosquito bite.
Asunto(s)
Anopheles/inmunología , Mordeduras y Picaduras de Insectos/inmunología , Interleucina-8/inmunología , Saliva/inmunología , Alérgenos/química , Alérgenos/aislamiento & purificación , Animales , Antígenos/química , Antígenos/aislamiento & purificación , Western Blotting , Factores Quimiotácticos Eosinófilos/inmunología , Cromatografía Líquida de Alta Presión , Relación Dosis-Respuesta Inmunológica , Electroforesis en Gel de Poliacrilamida , Eosinófilos/inmunología , Femenino , Humanos , Interleucina-8/química , Interleucina-8/aislamiento & purificación , Masculino , Ratones , Peso Molecular , Neutrófilos/inmunología , Glándulas Salivales/química , Glándulas Salivales/inmunologíaRESUMEN
A novel eosinophil chemotactic cytokine (ECF-L) was purified from the culture supernatant of splenocytes of mice by a combination of anion-exchange chromatography, Procion red-agarose affinity chromatography, size exclusion high performance liquid chromatography (HPLC), and reverse phase HPLC. The NH(2)-terminal amino acid sequence was determined by direct protein sequencing. An ECF-L cDNA clone of 1,506 nucleotides was isolated from a cDNA library, and the nucleotide sequence predicted a mature protein of 397 amino acids. A recombinant ECF-L showed a level of eosinophil chemotactic activity comparable with that of natural ECF-L, and the activity was inhibited by a monoclonal antibody to ECF-L. ECF-L also attracted T lymphocytes and bone marrow polymorphonuclear leukocytes in vitro, whereas it caused selective extravasation of eosinophils in vivo. ECF-L mRNA was highly expressed in spleen, bone marrow, lung, and heart. A comprehensive GenBank data base search revealed that ECF-L is a chitinase family protein. ECF-L retains those amino acids highly conserved among chitinase family proteins, but Asp and Glu residues essential for the proton donation in hydrolysis were replaced by Asn and Gln, respectively. Although ECF-L contains a consensus CXC sequence near the NH(2) terminus akin to chemokine family proteins, the rest of ECF-L shows poor homology with chemokines.
Asunto(s)
Infecciones por Cestodos/fisiopatología , Factores Quimiotácticos Eosinófilos/fisiología , Quitinasas/fisiología , Eosinófilos/fisiología , Neutrófilos/fisiología , Esquistosomiasis Japónica/fisiopatología , Transcripción Genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Infecciones por Cestodos/sangre , Quimiocinas CC/química , Quimiocinas CXC/química , Factores Quimiotácticos Eosinófilos/química , Factores Quimiotácticos Eosinófilos/genética , Quitinasas/química , Quitinasas/genética , Cromatografía Líquida de Alta Presión , Eosinófilos/parasitología , Femenino , Regulación de la Expresión Génica , Humanos , Linfocitos/química , Linfocitos/inmunología , Macrófagos/parasitología , Macrófagos/fisiología , Mesocestoides , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos , Datos de Secuencia Molecular , Neutrófilos/parasitología , ARN Mensajero/genética , Schistosoma japonicum , Esquistosomiasis Japónica/sangre , Alineación de Secuencia , Homología de Secuencia de Aminoácido , Bazo/inmunologíaRESUMEN
Production of eosinophil chemotactic factor by T-lymphocytes (ECF-L) was examined in Toxocara canis-infected mice. When spleen cells from T. canis-infected mice were cultured in serum-free RPMI1640, ECF-L production was detectable in an antigen-specific manner. The ECF-L production peaked at day 9 post-infection and then decreased. Depletion of Thy 1.2+ cells or CD8+ cells completely abrogated ECF-L production, whereas depletion of CD4+ cells did not, indicating that CD8+ T-cells are involved in the production of ECF-L. When bone marrow eosinophils obtained from T. canis-infected mice were preincubated with ECF-L, their chemotactic reactivity to parasite-derived ECFs was enhanced, whereas that of peritoneal cavity-derived eosinophils was not. Thus, ECF-L seems to be important not only as a chemoattractant but also as an activator of the chemotactic reactivity of naive eosinophils to the parasite-derived ECF in T. canis infection.
Asunto(s)
Linfocitos T CD8-positivos/metabolismo , Factores Quimiotácticos Eosinófilos/biosíntesis , Toxocara canis , Toxocariasis/inmunología , Animales , Antígenos Helmínticos , Médula Ósea , Células Cultivadas , Factores Quimiotácticos Eosinófilos/fisiología , Quimiotaxis de Leucocito , Eosinofilia/etiología , Eosinofilia/inmunología , Eosinófilos/fisiología , Femenino , Ratones , Ratones Endogámicos C57BL , Cavidad Peritoneal , Bazo/inmunología , Toxocariasis/complicacionesRESUMEN
Antibodies to a neutrophil chemotactic factor from Tritrichomonas foetus were used to screen a T. foetus cDNA expression library in lambda gt11. All positive clones were identified as homologs of iron-containing superoxide dismutase (SOD). Native gel electrophoresis showed that the antibodies indeed recognized T. foetus antigens with SOD activity. Two SOD genes were found in T. foetus, and cloned and sequenced as parts of larger genomic segments of 3844 and 4089 base pairs. Transcription initiated between the first and second methionine codons of each genomic open reading frame, generating mRNAs with 5' untranslated regions of 11-15 bases, and encoding proteins of 195 amino acids. The two SOD coding sequences lacked obvious introns. They were 79% identical at both the nucleotide and amino acid levels. Both SOD genes were inserted into a eukaryotic expression vector and stably expressed in mammalian cells; both proteins were recognized by the antibodies, and both assumed a cytosolic, extranuclear distribution in these cells. Histidine-tagged forms of both T. foetus SODs were expressed in E. coli and after purification, found to have neutrophil chemotactic activity similar to the non-recombinant factor purified from T. foetus. Identification of this neutrophil chemotactic factor as SOD provides additional insight into the host-parasite interaction.
Asunto(s)
Interleucina-8/química , Neutrófilos/parasitología , Superóxido Dismutasa/química , Tritrichomonas foetus/enzimología , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Cricetinae , Interleucina-8/genética , Interleucina-8/inmunología , Ratones , Datos de Secuencia Molecular , Neutrófilos/inmunología , Alineación de Secuencia , Homología de Secuencia de Aminoácido , Superóxido Dismutasa/genética , Superóxido Dismutasa/inmunología , Tritrichomonas foetus/genéticaRESUMEN
Experimental allergic encephalomyelitis (EAE) is an autoimmune disease inducible by encephalitogenic helper T cells expressing V beta 8.2. In this study, we examined the relationship between the stressor-induced alternation of clinical EAE and the induction of autoreactive T cells using Lewis rats. Animals were immersed for 5 min in a water bath maintained at 44 degrees C continuously for 10 or 13 days, before or after the immunization of the encephalitogenic peptide, respectively. Stress administrations after the immunization clearly diminished the severity of clinical EAE, and delayed the onset of disease. On the other hand, stress administrations prior to the immunization resulted in the marginal suppression of clinical EAE. Splenocytes of the stressed rats showed, however, comparative proliferative responses to the encephalitogenic peptide or mitogens with that of the control rats. Moreover, higher level of V beta 8.2 mRNA expression was detected in the spinal cords of the stressed rats than in control rats. Sequence analysis of CDR3 region of TCR cDNA showed that V beta 8.2+ T cells in the spinal cords of the stressed rats possess common features with the biased encephalitogenic T cells. These results suggest that the stressor-induced suppression of clinical EAE is not simply because of the failure of induction of autoreactive T cells, nor localization of the autoreactive T cells in the central nervous system.
Asunto(s)
Encefalomielitis Autoinmune Experimental/inmunología , Proteína Básica de Mielina/inmunología , Receptores de Antígenos de Linfocitos T alfa-beta , Receptores de Antígenos de Linfocitos T/inmunología , Estrés Psicológico/inmunología , Linfocitos T/inmunología , Secuencia de Aminoácidos , Animales , Autoanticuerpos/inmunología , Femenino , Activación de Linfocitos/fisiología , Datos de Secuencia Molecular , Proteína Básica de Mielina/biosíntesis , Reacción en Cadena de la Polimerasa , ARN Mensajero/biosíntesis , Ratas , Ratas Endogámicas Lew , Receptores de Antígenos de Linfocitos T/biosíntesis , Bazo/citologíaRESUMEN
The neutrophil is one of the sources of eosinophil chemotactic factor (ECF) in the presence of some stimulants. In the present study we showed that guinea-pig neutrophils could release ECF upon stimulation with Schistosoma japonicum eggs. ECF release from neutrophils began as early as 5 min after the stimulation and reached a peak at 20 min. When homogenate of the eggs was separated into a water-soluble fraction as soluble egg antigen (SEA) and a water-insoluble fraction (eggshell), both preparations possessed a potent neutrophil-stimulating activity to release ECF. The ECF release was dependent on the concentration of eggshells or SEA or on the number of neutrophils. The neutrophil-stimulating activity of eggshells was stable to heat, HCl, or pronase treatment but sensitive to NaOH treatment. When the eggs or eggshells were washed with acetone or Tween-20, they lost the neutrophil-stimulating activity to release ECF, indicating that the neutrophil-stimulating factor (NSF) possesses a lipid nature. The molecular weight of NSF extracted from the eggshells was estimated to be about 1000 Da by gel chromatography on Sephadex G25. The possible role of eggshells in the formation of eosinophil-rich granulomatous lesions in schistosomiasis japonica is discussed.
Asunto(s)
Antígenos Helmínticos/inmunología , Factores Quimiotácticos Eosinófilos/biosíntesis , Neutrófilos/metabolismo , Schistosoma japonicum/inmunología , Animales , Factores Quimiotácticos Eosinófilos/aislamiento & purificación , Cobayas , Ratones , Ratones Endogámicos BALB C , Óvulo/inmunologíaRESUMEN
The relationship between the cercarial allergen and two previously isolated egg allergens (J1, J2) of Schistosoma japonicum was examined especially in terms of the cross-reactivity between them. Semi-purified cercarial allergen (JAC) was obtained from the crude extract of S. japonicum cercariae by gel chromatography on Sephadex G-200. The apparent molecular weight of JAC was estimated approximately as 60-100 kDa. JAC could bind to Con A-Sepharose, indicating its glycoprotein nature. Three groups of BALB/c mice were immunized with JAC , J1 or J2 using A1(OH)3 as adjuvant, and the cross-reactivity of each anti-serum was examined by PCA. Anti-JAC, anti-J1 or anti-J2 serum was highly specific to the corresponding antigen. When IgE-ELISA of S. japonicum patient sera was performed using JAC, J1 or J2 as an antigen, the correlation between anti-J1 and anti-J2 (r = 0.78) was high, whereas the correlation between anti-JAC and anti-J1 (r = 0.27) or between anti-JAC and anti-J2 (r = 0.12) was low. These results suggest that most IgE epitopes on cercarial allergen are independent from those on egg allergens in S. japonicum.
Asunto(s)
Antígenos Helmínticos/análisis , Inmunoglobulina E/biosíntesis , Esquistosomiasis Japónica/inmunología , Esquistosomiasis/inmunología , Animales , Reacciones Cruzadas , Ensayo de Inmunoadsorción Enzimática , Epítopos , Femenino , Ratones , Ratones Endogámicos BALB C , Óvulo/inmunología , Sensibilidad y EspecificidadRESUMEN
The production of granulocyte-macrophage colony-stimulating factor (GM-CSF) by lymphocytes was examined in murine malaria. When spleen cells or lymph node cells from P. berghei-infected mice were cultured in vitro with malaria antigen, the GM-CSF production correlated with the incubation time up to 72 hours. When lymphocytes obtained at various days after infection were cultured with the antigen, GM-CSF became detectable as early as 2 days after infection, reached a peak at day 9 and then rapidly decreased. Production of GM-CSF was antigen-specific, and related to the dose of antigen. Treatment of lymphocytes with anti-Thy-1.2 antibody and complement resulted in almost complete loss of GM-CSF-producing activity, while treatment with either anti-CD4 or anti-CD8 antibody and complement resulted in partial loss of GM-CSF-producing activity, indicating that both CD4+ and CD8+ T cells are involved in GM-CSF production in malaria. GM-CSF exhibits glycoprotein nature, and has an apparent molecular weight of 36,000. The molecular properties of this T-cell derived GM-CSF were compared with those of known lymphokine GM-CSF.
Asunto(s)
Antígenos de Protozoos/metabolismo , Factor Estimulante de Colonias de Granulocitos y Macrófagos/biosíntesis , Malaria/inmunología , Plasmodium berghei/inmunología , Linfocitos T/inmunología , Animales , Cromatografía de Afinidad , Cromatografía Líquida de Alta Presión , Femenino , Ratones , Ratones Endogámicos C57BLRESUMEN
Infection of mice with Plasmodium berghei engendered a temporary appearance of granulocyte-macrophage colony-stimulating factor (GM-CSF) in the serum. The peak of GM-CSF levels was detected at day 2 post-infection, and then gradually decreased. On the other hand, the number of committed stem cells for granulocytes and macrophages (CFU-GM) in bone marrow transiently decreased at day 2 post-infection, and then increased and peaked at day 6 post-infection. When the serum of P. berghei-infected mice was fractionated by gel chromatography on Sephacryl S-300, GM-CSF activity was detected as a single peak with an apparent molecular weight of 64 KDa. GM-CSF was entirely adsorbed to concanavalin A-Sepharose 4B affinity chromatography, and was sensitive to pronase digestion, indicating its glycoprotein nature. These results suggest that the circulating GM-CSF would contribute the increase of granulocyte-macrophage hemopoiesis in the early phase of malaria.
Asunto(s)
Factor Estimulante de Colonias de Granulocitos y Macrófagos/sangre , Hematopoyesis/fisiología , Malaria/inmunología , Plasmodium berghei/patogenicidad , Animales , Modelos Animales de Enfermedad , Técnicas In Vitro , Malaria/parasitología , Ratones , Ratones Endogámicos , Factores de TiempoRESUMEN
Kinetic changes of eosinophil chemotactic factor (ECF) production from granulomas, splenic T-cells or mast cells were examined with reference to granuloma formation around newly deposited single eggs in Schistosoma japonicum-infected mice. The peri-ovular granulomas began to appear at around 5 weeks post-infection (p.i.). Their size reached a peak at 6 weeks and then decreased gradually. Up to 8 weeks p.i., eosinophils were the predominant cell type in the granulomas. ECF-release from isolated granulomas paralleled the size of granulomas. Circulating ECF-A, which was assumed to be derived from mast cells, was also detected 6 weeks afterwards in parallel with the level of specific IgE antibody level against egg antigens in the serum. The circulating ECF-A peaked at 8 weeks and decreased after 10 weeks. Spleen cells began to produce ECF specific to bone-marrow eosinophils began at 5 weeks p.i., reached a peak at 6 weeks and then decreased rapidly. On the other hand, the production of ECF specific to eosinophils obtained from the peritoneal cavity began at 6 weeks and decreased rapidly thereafter. These results suggest that various kinds of host-derived ECFs seem to contribute, in one way or an other, to the accumulation of eosinophils in and around granulomatous lesions. The possible role of these ECFs in eosinophil mobilization from the site of production to the inflamed site is discussed.
Asunto(s)
Factores Quimiotácticos Eosinófilos/biosíntesis , Eosinófilos , Granuloma/patología , Esquistosomiasis Japónica/metabolismo , Esquistosomiasis Japónica/patología , Animales , Anticuerpos Antihelmínticos/sangre , Células Cultivadas , Factores Quimiotácticos Eosinófilos/sangre , Eosinofilia , Femenino , Granuloma/metabolismo , Inmunoglobulina E/sangre , Cinética , Recuento de Leucocitos , Hígado/parasitología , Hígado/patología , Mastocitos/metabolismo , Ratones , Ratones Endogámicos C57BL , Óvulo , Schistosoma japonicum/inmunología , Schistosoma japonicum/fisiología , Esquistosomiasis Japónica/inmunología , Esquistosomiasis Japónica/parasitología , Bazo/metabolismoRESUMEN
A neutrophil chemotactic factor (TfNCF) was isolated from the crude extract of Tritrichomonas foetus organisms by a combination of anion-exchange chromatography on DE52 and gel filtration on Sephacryl S200. TfNCF showed homogenicity by both PAGE and SDS-PAGE. The molecular weight of TfNCF was estimated to be 22 and 24 kDa, by Sephacryl S200 gel chromatography and by SDS-PAGE under reducing conditions. Immunization of TfNCF caused almost complete protection against T. foetus infection in mice. Western blot analysis probed with anti-TfNCF antibody showed that the epitopes on TfNCF were not commonly shared on the other components of T. foetus organisms nor other helminthous parasite-derived components. Furthermore, pre-incubation of neutrophils with antigens of other helminthous parasites or N-formylmethionyl-leucyl-phenylalanine did not affect the neutrophil chemotactic activity for TfNCF. These results suggest that TfNCF is a novel NCF consisting of unique epitopes for both antigenicity and neutrophil chemotactic activity. The role of NCF in the initiation of the immune response is discussed.
Asunto(s)
Interleucina-8/análisis , Proteínas Protozoarias/análisis , Tritrichomonas foetus/química , Animales , Western Blotting , Cromatografía en Gel , Cromatografía por Intercambio Iónico , Electroforesis en Gel de Poliacrilamida , Femenino , Interleucina-8/aislamiento & purificación , Interleucina-8/fisiología , Ratones , Ratones Endogámicos , N-Formilmetionina Leucil-Fenilalanina/farmacología , Lavado Peritoneal , Proteínas Protozoarias/aislamiento & purificaciónRESUMEN
The immune responsiveness to specific antigens or mitogens was examined in jirds after primary and secondary infections with Brugia pahangi. When spleen cells were obtained from secondarily infected jirds, their proliferative responses to mitogens such as Con A or LPS, or to specific antigens prepared from infective larvae or adult worms were significantly lower than those of spleen cells obtained from primarily infected jirds. The proliferative responses of the peripheral blood mononuclear cells obtained from animals undergoing primary and secondary infections also showed a similar tendency. The depressed proliferative responses of the secondary infected spleen cells to Con A or LPS was partially restored by removing adherent/phagocytic cells from the original cell populations. After deletion of the adherent cells, however, antigen-specific proliferative responses were not altered and remained at low level. These results suggest that at least two different mechanisms of depression, namely adherent cell-mediated antigen-nonspecific suppression and unresponsiveness of lymphocytes to filarial antigens, are induced in jirds in the secondary infection.
Asunto(s)
Brugia pahangi , Filariasis/inmunología , Tolerancia Inmunológica , Enfermedades de los Roedores/inmunología , Animales , Antígenos Helmínticos/inmunología , Brugia pahangi/inmunología , Adhesión Celular/inmunología , División Celular/inmunología , Células Cultivadas , Epítopos , Gerbillinae , Inmunidad Innata , Larva/inmunología , Linfocitos/citología , Linfocitos/inmunología , Masculino , Bazo/citología , Bazo/inmunologíaRESUMEN
To compare the molecular structure of a parasite-derived neutrophil chemotactic factor (NCF) with host-derived NCFs or other NCFs, molecular cloning of cDNA encoding NCF derived from Dirofilaria immitis adult worm (DiNCF) was performed. A D. immitis cDNA library was screened with an antibody to DiNCF, and one DiNCF cDNA clone (pD-4) was isolated. A fusion protein of pD-4 and gene 10 protein showed significant neutrophil chemotactic activity whereas gene 10 protein itself showed marginal neutrophil chemotactic activity. The total nucleotide sequence analysis revealed that pD-4 was 994 bp long with a 432 bp open leading frame encoding a 143 residue protein. The NH2-terminal amino acid sequence of the natural DiNCF and the deduced amino acid sequence from the cDNA showed that the mature functional protein was comprised of 112 amino acids. Although the deduced amino acid sequence of this protein did not show overall homology to host-derived NCFs or other known proteins, it contained a similar sequence (Met-Phe-Lys) to the known chemotactic peptides. The possibility of the functional epitope of DiNCF is discussed.
Asunto(s)
Factores Quimiotácticos/genética , Dirofilaria immitis/inmunología , Neutrófilos/inmunología , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Western Blotting , Factores Quimiotácticos/biosíntesis , Factores Quimiotácticos/química , Factores Quimiotácticos/inmunología , Quimiotaxis de Leucocito , Clonación Molecular , Dirofilariasis/inmunología , Perros , Electroforesis en Gel de Poliacrilamida , Femenino , Biblioteca de Genes , Ratones , Datos de Secuencia Molecular , Plásmidos , ARN Mensajero/genética , Ratas , Ratas Endogámicas LewRESUMEN
In seven patients with paragonimiasis westermani, parasite-specific IgE and IgG levels in sera and pleural effusion were determined by an enzyme-linked immunosorbent assay (ELISA). The sensitivity to adult excretory-secretory (E-S) antigen was compared with the sensitivity to whole worm extract antigen, and the former was more sensitive in both an IgE-ELISA and IgG-ELISA. Both parasite-specific IgE and IgG could be detected by ELISA at levels much higher than those in control subjects using E-S antigen. When specific IgE and IgG levels in sera and pleural effusion of individual patients were compared, the latter had higher values. The difference between levels of specific IgE in pleural effusion and serum did not correlate with that of specific IgG. These results indicate that specific IgE and IgG antibodies form locally, i.e., in the lung, and that pleural effusions from patients with paragonimiasis are more suitable than serum for immunodiagnosis.
Asunto(s)
Inmunoglobulina E/análisis , Inmunoglobulina G/análisis , Paragonimiasis/inmunología , Paragonimus/inmunología , Derrame Pleural/inmunología , Animales , Anticuerpos Antihelmínticos/análisis , Anticuerpos Antihelmínticos/sangre , Ensayo de Inmunoadsorción Enzimática , Humanos , Inmunoglobulina E/sangre , Inmunoglobulina G/sangreRESUMEN
We examined the effect of adherent cells from bone marrow or spleen of mice infected with Plasmodium berghei on dyserythropoiesis. Significant reduction in number of erythroid progenitors (erythroid colony-forming units: CFU-E and erythroid burst-forming units: BFU-E) was observed in bone marrow as early as 1 day after P. berghei infection. When adherent cells were removed from bone marrow or spleen cells of infected mice, the number of CFU-E and BFU-E was clearly increased. Furthermore, addition of adherent cells from infected mice to nonadherent cells from normal mice inhibited erythroid colony formation significantly in a dose-dependent manner. These results suggest that the adherent cells obtained from bone marrow or spleen of mice in the early stage of P. berghei-infection have a suppressive effect on erythropoiesis.
Asunto(s)
Células Precursoras Eritroides/inmunología , Eritropoyesis/inmunología , Malaria/inmunología , Plasmodium malariae/inmunología , Animales , Células de la Médula Ósea , Femenino , Humanos , Lactante , Ratones , Plasmodium malariae/citología , Bazo/citología , Factores Supresores Inmunológicos/fisiologíaRESUMEN
The kinetic changes of hemopoietic stem cells in bone marrow and spleen were compared between lethal Plasmodium berghei- and non-lethal P. yoelii 17x-infected mice. P. yoelii 17x-infected mice showed more severe splenomegaly than those infected with P. berghei. P. yoelii 17x-infected mice also showed a greater degree of sustained increase in number of multipotent hemopoietic stem cells (colony-forming units in spleen: CFU-S) and committed stem cells for granulocytes and macrophages (CFU-GM) and for erythrocytes (CFU-E) than P. berghei-infected mice. Such an increase was predominantly seen in the spleen of P. yoelii 17x-infected mice. In P. berghei-infected mice, the number of CFU-S, CFU-GM and also CFU-E only transiently increased and then decreased to a subnormal level at the late stage of infection. The proportion of cycling CFU-S was higher in P. berghei-infected mice than in P. yoelii 17x-infected mice. The IL-3 producing activity per spleen was much higher in P. yoelii 17x-infected than in P. berghei-infected mice at any point in time during the infection. Thus, hemopoietic changes seen after malaria infection seem to be closely related to the pathogenicity of the malaria parasite.
Asunto(s)
Células Madre Hematopoyéticas/citología , Malaria/sangre , Plasmodium berghei/patogenicidad , Plasmodium yoelii/patogenicidad , Animales , Células de la Médula Ósea , Femenino , Ratones , Ratones Endogámicos C57BL , Bazo/citología , VirulenciaRESUMEN
The allergens of the lung fluke Paragonimus westermani were localized by indirect immunostaining in adult fluke sections using pleural exudates from 3 patients with P. westermani. Immunostaining performed by using pleural exudate with the highest level of specific IgE revealed that the P. westermani major allergen (or allergens) was located in the gut epithelium and luminal contents and that minor allergens were in the tegument and parenchyma. The antigens recognized by specific IgG were located at various sites including those recognized by specific IgE. Paragonimus westermani-specific IgE cross-reacted with only the gut of 2 other Paragonimus species, Paragonimus miyazakii and Paragonimus ohirai. The major allergen in the gut also was recognized by the other 2 pleural exudates. These results indicate that the substance present in and secreted from the gut is not only a major allergen but is also a common allergen among Paragonimus species.
Asunto(s)
Alérgenos/análisis , Paragonimiasis/inmunología , Paragonimus/inmunología , Pleura/inmunología , Animales , Reacciones Cruzadas , Técnica del Anticuerpo Fluorescente , Humanos , Técnicas para Inmunoenzimas , Inmunoglobulina E/inmunología , Inmunoglobulina G/inmunologíaRESUMEN
The susceptibility of haemopoietic stem cell deficient W/Wv mice to infection with Plasmodium berghei was examined. The mean survival time of W/Wv mice after the infection was shorter than that of the +/+ mice. Splenomegaly, a characteristic pathological change of the host after infection with malaria parasites was not observed in W/Wv mice. When haemopoietic activity of the infected mice was examined, a substantial increase in number of multipotent haemopoietic stem cells (CFU-S) and the committed stem cells for granulocytes and macrophages (CFU-GM) or for erythrocytes (CFU-E) was observed in the bone marrow and spleen of +/+ but not of W/Wv mice. CFU-S were not detected in W/Wv mice before or after infection. The number of CFU-GM and CFU-E in bone marrow and spleen of W/Wv mice decreased after infection. Bone marrow grafting from +/+ to W/Wv mice 8 weeks before infection prolonged the mean survival time of the mice and effectively restored the number of CFU-S in the spleen of W/Wv mice. These results indicate that multi-potent haemopoietic stem cells play an important role in the host's defence mechanisms against P. berghei-infection.
Asunto(s)
Células Madre Hematopoyéticas/inmunología , Malaria/etiología , Plasmodium berghei , Anemia Macrocítica/complicaciones , Anemia Macrocítica/genética , Anemia Macrocítica/inmunología , Animales , Médula Ósea/inmunología , Médula Ósea/patología , Trasplante de Médula Ósea/inmunología , Trasplante de Médula Ósea/patología , Células Madre Hematopoyéticas/patología , Malaria/complicaciones , Malaria/inmunología , Masculino , Mastocitos/inmunología , Mastocitos/patología , Ratones , Ratones Mutantes , Bazo/inmunología , Bazo/patologíaRESUMEN
Extramedullary hemopoiesis, recognized as hemopoietic foci, increased in the livers of Toxocara canis-infected mice. At the peak of the response (day-13 after infection), the majority of hepatic hemopoietic foci were of the eosinophil lineage. Hepatic nonparenchymal cells prepared from T. canis-infected mice on day 13 contained large numbers of hemopoietic stem cells, more than half of which were cycling. When W/Wv mice, which are genetically deficient in multipotent hemopoietic stem cells, were infected with T. canis, hepatic hemopoietic foci were rare throughout the course of infection. This impaired response of W/Wv mice was restored by bone marrow grafting from normal +/+ littermates. These results indicate that, in response to the increased demand, eosinophils are generated in the liver by the differentiation from multipotent stem cells, not only from the committed precursors.