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1.
Pesqui. vet. bras ; 36(7): 652-656, jul. 2016. tab, graf, ilus
Article in English | LILACS, VETINDEX | ID: lil-794775

ABSTRACT

The thymus is a lymphoid organ and usually evaluated for the degree of lymphocyte loss with subjective histological techniques. This study aimed to adapt and to apply of the digital analysis of the lymphoid depletion system (ADDL) in the thymus in order to obtain a more accurate analysis. Glucocorticoid was used to induce immunosuppression in 55 broilers at 21 days of age; other 15 broilers were the control group. After euthanasia of the broilers, postmortem examination was made. Both thymic chains were collected and six lobes were selected for histological examination of the degree of lymphocyte depletion (scores 1 to 5) and for submission to all stages of processing by the ADDL system. The artificial constructed neural networks (ANN) obtained 94.03% of correct classifications. In conclusion, it was possible to adopt objective criteria to evaluate thymic lymphoid depletion with the ADDL system.(AU)


O timo é um órgão linfóide, que é normalmente avaliado para o grau de perda de linfócitos a partir de técnicas histológicas subjetivas. Este trabalho teve como objetivo a adaptação e aplicação do sistema de análise digital de depleção linfóide (ADDL) para o timo, a fim de tornar sua análise mais acurada. Glicocorticóides foram utilizados a fim de induzir imunossupressão em 55 aves de 21 dias de idade. Outras 15 aves formaram o grupo controle. Posteriormente, para cada um dos aves, realizou-se a eutanásia e necropsia. Ambas as cadeias do timo foram coletadas e foram selecionadas seis lóbulos para processamento histológico, análise quanto ao grau de depleção linfocitária (escores de 1-5) e submissão a todas as fases do processamento pelo sistema ADDL. Observou-se que a rede neural artificial (RNA) construída obteve 94,03% de classificações corretas. Em conclusão, foi possível adotar critérios objetivos para avaliar a depleção linfóide tímica utilizando o sistema ADDL.(AU)


Subject(s)
Animals , Chickens/physiology , Immunity, Cellular/physiology , Lymphocyte Depletion/veterinary , Lymphocytes/physiology , Nerve Net/physiology , Thymus Gland/physiopathology , Glucocorticoids/analysis
2.
J. appl. oral sci ; 20(5): 503-509, Sept.-Oct. 2012. graf, tab
Article in English | LILACS | ID: lil-654912

ABSTRACT

Phagocytosis by neutrophils and monocytes constitutes the main defense mechanism against bacterial challenges in periodontitis. Phagocytosis by neutrophils has already been evaluated, whereas phagocytic function of monocytes has hardly been addressed so far. Objectives: The aim of this study was to assess phagocytosis by neutrophils and monocytes in periodontitis. Material and Methods: The sample included 30 subjects with severe periodontitis and 27 control subjects without periodontal disease. The phagocytic index (PhI) was calculated as the mean number of adhered/ingested Saccharomyces cerevisiae per phagocytozing monocyte or neutrophil multiplied by the percentage of phagocytes involved in phagocytosis. Results: A significant reduction in phagocyte functions was observed in individuals with periodontitis. The median of PhI of neutrophils using nonsensitized S. cerevisiae was 3 for the control group, and 1.5 for the periodontitis group (p=0.01, Mann-Whitney test). The median of PhI of monocytes with non-sensitized S. cerevisiae was 26.13 for the control group, and 13.23 for the periodontitis group (p=0.03, Mann Whitney test). The median of PhI of monocytes assessed with sensitized S. cerevisiae was 97.92 for the control group and 60.1 for the periodontitis group (p=0.005, t-test). Conclusion: The data demonstrated a reduction in the function of phagocytes, suggesting a decrease in immune defenses in periodontitis.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Young Adult , Monocytes/physiology , Neutrophils/physiology , Periodontitis/immunology , Phagocytosis/physiology , Case-Control Studies , Immunity, Cellular/physiology , Periodontitis/blood , Statistics, Nonparametric , Saccharomyces cerevisiae/cytology
3.
Pesqui. vet. bras ; 29(9): 725-730, Sept. 2009. ilus
Article in Portuguese | LILACS | ID: lil-532843

ABSTRACT

Um experimento foi conduzido para avaliar o efeito de níveis crescentes de parede de levedura e idade das matrizes reprodutoras sobre o peso dos órgãos linfóides, a resposta imune celular e o perfil hematológico de frangos de corte. Foram utilizados 3.360 pintos de corte da linhagem Cobb, distribuídos em delineamento inteiramente casualisado, em esquema fatorial 2x5, mais dois controles, sendo duas idades de matrizes (34 e 57 semanas de idade) e cinco níveis de suplementação de parede de levedura (zero, um, dois, três e quatro kg de parede de levedura/tonelada de ração). A idade das matrizes influenciou a resposta de todas as variáveis. A inclusão de 3kg de parede de levedura/tonelada de ração promoveu, na progênie de reprodutoras de 57 semanas, reação inflamatória mais intensa quando comparada a dieta controle, no entanto não houve aumento significativo no número de heterófilos e linfócitos circulantes. Conclui-se que a utilização da parede de levedura associada ao sorgo ou não em rações de frangos de corte ainda necessita de estudos complementares, que incluam, por exemplo, os componentes purificados da parede de levedura (MOS e ß-glucano).


An experiment was carried out to evaluate the effect increasing levels of yeast wall and broiler breeders' age levels on lymphoid organs weight, cellular immune response and hematological parameters in broilers. A total of 3,360 Cobb broilers were allotted, in a completely randomized design and a 2x5 factorial arrangement, and two controls, compound of two broiler breeders age (34 and 57 weeks of age) and five yeast wall levels (zero, one, two, three and four kg of yeast wall/ton of diet). Broiler breeders' age affected all studied variables. The inclusion of 3kg of yeast wall/ton of meal increased, at 57 weeks age broiler breeders, more intense inflammatory reaction when compared to control diet; however the circulated heterophils and lymphocytes numbers were not increased. In conclusion, the use of yeast wall, associated or not to sorghum on broilers diet still needs complementary studies, for example, purified components of yeast wall (MOS and ß-glucano).


Subject(s)
Animals , Poultry/growth & development , Immunity, Cellular/physiology , Yeasts/cytology , Sorghum/metabolism , Poultry/immunology , Immunologic Factors/analysis , Infant Nutritional Physiological Phenomena/supply & distribution
4.
Braz. j. med. biol. res ; 38(10): 1475-1486, Oct. 2005. ilus
Article in English | LILACS | ID: lil-409276

ABSTRACT

Two different levels of control for bone marrow hematopoiesis are believed to exist. On the one hand, normal blood cell distribution is believed to be maintained in healthy subjects by an "innate" hematopoietic activity, i.e., a basal intrinsic bone marrow activity. On the other hand, an "adaptive" hematopoietic state develops in response to stress-induced stimulation. This adaptive hematopoiesis targets specific lineage amplification depending on the nature of the stimuli. Unexpectedly, recent data have shown that what we call "normal hematopoiesis" is a stress-induced state maintained by activated bone marrow CD4+ T cells. This T cell population includes a large number of recently stimulated cells in normal mice whose priming requires the presence of the cognate antigens. In the absence of CD4+ T cells or their cognate antigens, hematopoiesis is maintained at low levels. In this review, we summarize current knowledge on T cell biology, which could explain how CD4+ T cells can help hematopoiesis, how they are primed in mice that were not intentionally immunized, and what maintains them activated in the bone marrow.


Subject(s)
Animals , Humans , Bone Marrow Cells/cytology , /immunology , Hematopoiesis/immunology , Immunologic Memory/immunology , Bone Marrow Cells/immunology , /physiology , Immunity, Cellular/physiology , Immunity, Innate/physiology , Immunologic Memory/physiology
5.
Rev. chil. reumatol ; 21(2): 58-64, 2005. graf
Article in Spanish | LILACS | ID: lil-432947

ABSTRACT

Autoinmune diseases occur when the immunological system loses its capability to recognize between self and foreign, and develops a response against healthy tissues. Both molecular bases that trigger these pathologies and genetic factors of susceptibility are unknown. Identification of these factors is fundamental for understanding and developing specific therapies for autoimmune diseases. Dendritic cells (DCs) - professional antigen presenting cells - play a fundamental roll in the development and modulation of the acquired immune response because they have the unique capacity to active naïve T lymphocytes. In order to activate T lymphocytes, the DCs must supply simultaneously two molecular signals which correspond to the antigen (or peptid complex MHC) plus costimulating signals. In absence of costimulation, the DCs induce inactivation of T lymphocytes, mechanism by which they are able to maintain peripheral tolerance against self antigens. In this way, it has been proposed that the immature DCs present antigens in absence of costimulation and provoke tolerance. On the contrary, mature DCs present antigens together with costimulating signals, which lead to immunity. In self-immune diseases, the process of tolerance in the presence of autoantigens could be deficient due to alterations in the normal function of DCs. One of the causes of this defect could be that there is an unbalance in the expression of activating and inhibiting Fcy receptors on the surface of DCs. This would generate DCs with a constitutive phenotype of maturity that would interfere with its tolerogenic activity, and would favor the permanent activation of T lymphocytes, including those that are autoreactive.


Subject(s)
Humans , Autoimmunity , Lymphocyte Activation/physiology , Dendritic Cells/immunology , Immunity, Cellular/physiology , Antigen Presentation , Lymphocyte Activation/immunology , Autoimmune Diseases/etiology , T-Lymphocytes/immunology , Immune Tolerance/physiology
6.
Salud pública Méx ; 46(1): 64-70, ene.-feb. 2004. tab
Article in Spanish | LILACS | ID: lil-361844

ABSTRACT

Los gametocitos de Plasmodium son los responsables de la transmisión del huésped vertebrado al mosquito vector. Sufren un proceso de desarrollo complejo a partir de parásitos asexuales, que no está completamente entendido, expresando proteínas y moléculas de adhesión específicas. Son capaces de inducir una respuesta inmune humoral específica con anticuerpos IgG, y celular específica, con producción de TNFa, IFNg y proliferación de linfocitos gd+, aun cuando existen respuestas inducidas en contra de las etapas previas del parásito (esporozoito, exo-eritrocítica y eritrocítica). Las vacunas destinadas a bloquear la transmisión del parásito no contemplan a los gametocitos circulantes en el huésped como blancos de acción, sino que van enfocadas contra antígenos expresados en los gametos y en las etapas posfertilización. El estudio de los mecanismos que regulan la producción de gametocitos y de la respuesta inmune contra éstos, ofrece una oportunidad para el desarrollo de estrategias adicionales para el control de la transmisión.


Subject(s)
Animals , Humans , Life Cycle Stages , Malaria Vaccines , Plasmodium falciparum/growth & development , Plasmodium falciparum/immunology , Plasmodium vivax/growth & development , Plasmodium vivax/immunology , Antibody Formation/physiology , Immunity, Cellular/physiology
7.
Biocell ; 27(2): 197-203, Aug. 2003.
Article in English | LILACS | ID: lil-384243

ABSTRACT

The defense reactions against biological (Histoplasma capsulatum and Escherichia coli) and non-biological materials (China ink and nylon thread) were tested in vivo in third instar larvae of Dermatobia hominis. The cellular defense performed by larval hemocytes was observed under electron microscopy. China ink particles were phagocytosed by granular cells 5 h after injection. E. coli cells were internalized by granular cells as early as 5 min after injection and totally cleared 180 min post-injection, when many hemocytes appeared disintegrated and others in process of recovering. H. capsulatum yeasts provoked, 24 h after being injected, the beginning of nodule formation. Nylon thread was encapsulated 24 h after the introduction into the hemocoel. Our results suggest that granular cells were the phagocytic cells and also the responsible for the triggering of nodule and capsule formation. In the presence of yeasts cells and nylon thread, they released their granules that chemotactically attracted the plasmatocytes that on their turn, flattened to surround and isolate the foreign material.


Subject(s)
Diptera/immunology , Phagocytes/immunology , Hemocytes/immunology , Immunity, Cellular/physiology , Larva/immunology , Diptera/microbiology , Escherichia coli/immunology , Phagocytes/ultrastructure , Phagocytosis/immunology , Hemocytes/ultrastructure , Histoplasma/immunology , Ink , Larva/microbiology , Microscopy, Electron , Chemotaxis/immunology , Reaction Time/immunology
8.
Article in English | IMSEAR | ID: sea-39944

ABSTRACT

The aim of the exercise was to improve body health including the immune system function. However, several studies have observed the suppression of immune response in athletes who were trained with strenuous exercise. Recruits who have been in the recruitment-training program for 8 weeks might also have immune suppression. Twenty males, aged from 21 to 23 years in Chulachomklao Royal Military Academy infantry battalion volunteered to participate in this study. They were asked to wear a Polar Accurex Plus Telemetric heart rate monitor during the training period. Tuberculin skin test which is the screening method for cellular immune responses was significantly decreased at post-training compared to the pre-training (p<0.02). The levels of serum IgG and IgM at pre-training, 4th week, 8th week and one week post-training were significantly decreased at the initiation period, which were compared with pre-training and 4th week of training (p<0.01), and returned to normal at the 8th week of training and one week post-training. The level of circulating immune cells and number of CD markers (CD3, CD4, CD8, and CD56) were not significantly changed throughout the training period. This study demonstrated that subjects who underwent the recruit-training program were able to improve their health after the period of training i.e., in the adaptation period. The decrease in the initiation period could be compensated with proper diet and enough rest.


Subject(s)
Adult , Analysis of Variance , Antibody Formation/physiology , Antigens, CD/analysis , Blood Chemical Analysis , Cohort Studies , Exercise/physiology , Humans , Immunity, Cellular/physiology , Immunocompetence/physiology , Military Personnel , Oxygen Consumption , Physical Education and Training , Probability , Respiratory Function Tests , Thailand , Tuberculin Test
9.
Indian J Exp Biol ; 2001 Sep; 39(9): 878-82
Article in English | IMSEAR | ID: sea-57686

ABSTRACT

In a bid to characterize the antigens and immunization mechanisms which may be used to produce a protective response against L. donovani, role of lipid associated polysaccharide (LPS) antigen and whole antigen was evaluated. BALB/C mice were immunized with whole or LPS antigen in combination with one of three putative adjuvents (anti CD-2 antibody/FIA/0.85% Saline). LPS antigen emulsified in anti CD-2 antibody was found to induce significant antibodies in mice on day 28 against challenge with lethal dose of L. donovani. Immunoprophylactic properties of LPS and whole antigen was investigated on day 40 through cytokine elicitation (IL-2), MIF) in culture supernatants of spleen cells, but before that MHC-II expressed on macrophage was studied. The LPS antigen in combination with anti CD-2 antibody was found to be most immuno-reactive inducing higher MHC-II expression on macrophages which was associated with substantial rise in the level of MIF and IL-2. It coincided with decline in antibody titre in 100% mice immunized with LPS antigen while Leishmania injected as whole antigen failed to induce specific macrophage and T-cell response with all the above formulations. We surmise from our data that lipid associated polysaccharide antigen linked to anti CD-2 antibody has potential for eliciting protective immunity against Leishmania.


Subject(s)
Animals , Antibodies, Monoclonal/immunology , Antibodies, Protozoan/biosynthesis , CD2 Antigens/immunology , Antigens, Protozoan/immunology , Histocompatibility Antigens Class II/immunology , Immunity, Cellular/physiology , Immunization , Interleukin-2/metabolism , Leishmania donovani/immunology , Leishmaniasis, Visceral/immunology , Lipopolysaccharides/immunology , Macrophages/parasitology , Mice , Mice, Inbred BALB C , T-Lymphocytes/physiology
10.
Acta bioquím. clín. latinoam ; 35(1): 37-61, mar.2001. ilus
Article in Spanish | LILACS | ID: lil-289154

ABSTRACT

Todos los microorganismos (bacterias, parásitos, hongos y virus) han constituido desde siempre un panel de agresores para el hombre, siendo responsables directos o indirectos de múltiples patologías de origen infeccioso que se desarrollan enfrentando a los mecanismos de la inmunidad. El presente artículo se divide en dos partes: la primera constituye una resumida actualización de los eventos inmunes y la segunda una discusión de la relación microbios-hombre en términos evolutivos replanteando desde esa óptica el clásico antagonismo. En ese sentido, un dinámico equilibrio entre ambos, puede ser alternativamente alterado por uno de los responsables con una consecuente compensación a cargo de la contraparte. Así, tomando como referencia el permanente cambio en las estrategias de evasión microbiana, puede especularse que los mecanismos inespecíficos junto a las barreras naturales pueden haber sido la defensa ancestral del hombre. Más adelante la inflamación inicial puede haber sido mejorada mediante la generación de moléculas activadoras del complemento. Posteriormente, las moléculas de histocompatibilidad y los receptores antigénicos de los linfocitos B y de los linfocitos T pueden haber sido generadas para montar los eventos específicos que hoy se conocen. La participación de células fundamentales y accesorias en forma conjunta ha hecho necesaria la expresión de moléculas de adhesión y la generación y ampliación del espectro de citoquinas y sus receptores. La producción de anticuerpos puede haber inducido el mejoramiento efector de sistemas moleculares como el complemento y así juntos, eficientizar la primitiva fagocitosis. La evolución del linaje T puede haber sido más compleja, habida cuenta que debieron generarse subpoblaciones o sets citotóxicos por un lado y orquestadores y reguladores por otro. Por otra parte la diversidad de reconocimiento que se hizo necesaria a nivel de los receptores específicos se desarrolló con un gasto mínimo de información genética, pero posibilitó la aparición de fenómenos no deseados con participación de efectores inmunes, lo que impuso la aparición de críticos mecanismos reguladores donde participan sinérgicamente todos los sistemas biológicos...


Subject(s)
Humans , Immunity, Active/physiology , Immunity, Innate/physiology , Inflammation/physiopathology , Inflammation Mediators/physiology , Bacteria/pathogenicity , Cell Adhesion Molecules , Killer Cells, Natural , Complement System Proteins/immunology , Cytokines , Antibody Formation/physiology , Immunity, Cellular/physiology , Immunity, Mucosal/physiology , Lymphocytes/immunology , Mast Cells , Phagocytes/immunology
11.
Article in English | IMSEAR | ID: sea-39984

ABSTRACT

A study was carried out in Thailand to determine the frequency of reactivity to delayed-type hypersensitivity (DTH) skin tests used for the staging of HIV patients in the United States. A four-antigen panel which included tetanus toxoid (1:10), Candida (1:10), mumps and Trichophyton antigens was assessed in 221 adult subjects from across the full immunological spectrum of HIV disease. Complete anergy was found in 38 per cent of 73 subjects with CD4 counts of 0-200 cells/ml and in 6 per cent of 78 subjects with 201-400 cells/ml. Partial anergy (response to 1 of 4 antigens) was found in 26 per cent of the 0-200 cell/ml group and decreased progressively with increasing CD4 cell count. Results suggested that a 3-member recall antigen panel would provide nearly all the clinically useful information gained by the more standard 4-member panel. In conclusion, DTH skin testing was confirmed to provide a method of assessing the integrity of cellular immune function of HIV-infected Thai adults which correlated with disease progression.


Subject(s)
Adult , Antigens, Bacterial/diagnosis , Antigens, Fungal/diagnosis , Antigens, Viral/diagnosis , Biomarkers/analysis , CD4 Lymphocyte Count , Chi-Square Distribution , Female , HIV Infections/diagnosis , Humans , Hypersensitivity, Delayed/epidemiology , Immunity, Cellular/physiology , Male , Prognosis , Sensitivity and Specificity , Severity of Illness Index , Skin Tests , Thailand
12.
Braz. j. med. biol. res ; 33(4): 365-8, Apr. 2000. ilus
Article in English | LILACS | ID: lil-258178

ABSTRACT

Gap junctions are clusters of intercellular channels directly connecting the cytoplasm of adjacent cells. These channels are formed by proteins named connexins and are present in all metazoan organisms where they serve diverse functions ranging from control of cell growth and differentiation to electric conduction in excitable tissues. In this overview we describe the presence of connexins in the cardiovascular and lympho-hematopoietic systems giving the reader a summary of the topics to be covered throughout this edition and a historical perspective of the discovery of gap junctions in the immune system


Subject(s)
Humans , Connexins/physiology , Gap Junctions/physiology , Immunity, Cellular/physiology , Myocardium/cytology , Cell Communication/physiology , Heart/physiology , Muscle, Smooth, Vascular/cytology , Muscle, Smooth, Vascular/physiology , Myocardium/chemistry
13.
Braz. j. med. biol. res ; 33(4): 447-55, Apr. 2000. ilus
Article in English | LILACS | ID: lil-258180

ABSTRACT

Gap junction channels are sites of cytoplasmic communication between contacting cells. In vertebrates, they consist of protein subunits denoted connexins (Cxs) which are encoded by a gene family. According to their Cx composition, gap junction channels show different gating and permeability properties that define which ions and small molecules permeate them. Differences in Cx primary sequences suggest that channels composed of different Cxs are regulated differentially by intracellular pathways under specific physiological conditions. Functional roles of gap junction channels could be defined by the relative importance of permeant substances, resulting in coordination of electrical and/or metabolic cellular responses. Cells of the native and specific immune systems establish transient homo- and heterocellular contacts at various steps of the immune response. Morphological and functional studies reported during the last three decades have revealed that many intercellular contacts between cells in the immune response present gap junctions or "gap junction-like" structures. Partial characterization of the molecular composition of some of these plasma membrane structures and regulatory mechanisms that control them have been published recently. Studies designed to elucidate their physiological roles suggest that they might permit coordination of cellular events which favor the effective and timely response of the immune system


Subject(s)
Humans , Connexins/physiology , Gap Junctions/physiology , Immune System/cytology , Immune System/physiology , Bone Marrow Cells/cytology , Cell Communication/physiology , Immunity, Cellular/physiology , Stromal Cells/physiology
14.
In. Timerman, Ari; Machado César, Luiz Antonio; Ferreira, Joäo Fernando Monteiro; Bertolami, Marcelo Chiara. Manual de Cardiologia: SOCESP. Säo Paulo, Atheneu, 2000. p.28-31, ilus.
Monography in Portuguese | LILACS | ID: lil-265378
15.
Rev. mex. pueric. ped ; 6(36): 302-10, jul.-ago. 1999. tab, ilus
Article in Spanish | LILACS | ID: lil-276185

ABSTRACT

Los niños que padecen síndrome nefrótico (SN) presentan una alta incidencia de peritonitis, una complicación infecciosa grave. Se revisan los factores involucrados en la génesis de la peritonitis primaria. Asimismo, se propone una ruta diagnóstica y terapéutica accesible para el médico general, el pediatra y el nefrólogo. Se describen las recomendaciones en materia de prevención. Se concluye que el diagnóstico de peritonitis primaria debe considerarse en todo paciente con SN idiopático que desarrolle abdomen agudo indicativo de apendicitis aguda


Subject(s)
Humans , Child , Appendicitis , Peritonitis/etiology , Peritonitis/physiopathology , Peritonitis/therapy , Nephrotic Syndrome/complications , Nephrotic Syndrome/diagnosis , Nephrotic Syndrome/therapy , Peritonitis/mortality , Immunity, Cellular/physiology , Nephrotic Syndrome/prevention & control
16.
J. Health Sci. Inst ; 17(1): 19-26, jan.-jun. 1999. tab, graf
Article in Portuguese | LILACS | ID: lil-282781

ABSTRACT

O presente trabalho procurou analisar uma metodologia de avaliação da resposta imune em ovinos mantidos em condições experimentais. Foram empregados cinqüenta ovinos adultos divididos em cinco grupos experimentais. Os animais foram tratados com levamisol (grupo I), parapoxvirus (Grupo II) e dexametasona (grupo III). Os grupos IV e V foram usados com controle. A resposta imune celular foi analisada pelo teste da tuberculina após sensibilização prévia pelo BCG. A resposta imune humoral foi analisada pelo teste de soroaglutinação em placa após a sensibilização pela vacina contra a brucelose. A sensibilização prévia de ovinos com BCG e com a vacina contra a brucelose pôde ser posteriormente comprovada, todavia, não foi possível demonstrar diferenças nestas respostas em animais tratados com levamisol, parapoxvirus e dexametasona.


Subject(s)
Animals , Male , Autoimmunity , Brucellosis/immunology , Immune System , Models, Animal , Mycobacterium bovis/immunology , Dexamethasone/therapeutic use , Antibody Formation/physiology , Immunity, Cellular/physiology , Levamisole/therapeutic use , Parapoxvirus , Sheep , Tuberculin
18.
Braz. j. med. biol. res ; 31(1): 89-104, Jan. 1998. ilus
Article in English | LILACS | ID: lil-212543

ABSTRACT

Toxoplasma gandii and Trypanosoma cruzi are intracellular parasites which, as part of their life cycle, induce a potent cell-mediated immunity (CMI) maintained by Th1 lymphocytes and IFN-gamma. In both cases, induction of a strong CMI is thought to protect the host against rapid parasite multiplication and consequent pathology and lethality during the acute phase of infection. However, the parasitic infection is not eliminated by the immune system and the vertebrate host serves as a parasite reservoir. In contrast, Leishmania sp, which is a slow growing parasite, appears to evade induction of CMI during early stages of infection as a strategy for surviving in a hostile environment (i.e., inside the macrophages which are their obligatory niche in the vertebrate host). Recent reports show that the initiation of IL-12 synthesis by macrophages during these parasitic infections is a key event in regulating CMI and disease outcome. The studies reviewed here indicate that activation/inhibition of distinct signaling pathways and certain macrophage functions by intracellular protozoa are important events in inducing/modulating the immune response of their vertebrate hosts, allowing parasite and host survival and therefore maintaining parasite life cycles.


Subject(s)
Immunity, Cellular/physiology , Protozoan Infections/immunology , Protozoan Infections/physiopathology , Cytokines/physiology , Leishmania , Toxoplasma , Trypanosoma cruzi
19.
Medicina (B.Aires) ; 58(6): 713-6, 1998. ilus, tab
Article in Spanish | LILACS | ID: lil-228222

ABSTRACT

Se investigó la presencia de la 5 isoenzima de la fosfatasa ácida leucocitaria tartrato resistente (FATRE) en los monocitos de sangre periférica humana en 32 muestras: 26 normales, 4 plaquetopenias, 1 anemia y 1 tricoleucemia. Se empleó el separador celular Cobe Spectra Versión 4 en 3 muestras y en las demás se obtuvo la concentración celular por centrifugación sin y con partículas de látex, para estudiar monocitos y macrófagos, respectivamente. Empleando el Kit Sigma para las dos reacciones de fosfatasa ácida total y de FATRE, se demostró la presencia de dos poblaciones de monocitos, una minoritaria para FATRE y otra negativa. Con la adición de látex los monocitos se transformaron en macrófagos haciéndose fuertemente positivos para FATRE. En consecuencia se concluye que la FATRE debe desempeñar un papel principal en la función macrofágica y por ende en la inmunidad celular humana.


Subject(s)
Humans , Acid Phosphatase/physiology , Immunity, Cellular/physiology , Leukocytes/enzymology , Macrophages/enzymology , Monocytes/enzymology , Tartrates/metabolism , Acid Phosphatase/metabolism , Cell Separation , Latex
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