Effect of fresh frozen plasma on the in vitro activation of U937 monocytes: a potential role for the age of blood donors and their underlying cytokine profile

BACKGROUND: Fresh frozen plasma (FFP) administration may increase the risk of nosocomial infections in parallel with the development of immune modulation. This could be driven by soluble mediators, possibly influencing the in vitro activation of human U937 monocyte cells, in a manner dependent on the age of the donors. METHODS: FFP donors were stratified into groups of 19-30 years, 31-40 years or 41-50 years, and U937 cells were cultured with FFP (alone or plus lipopolysaccharide-LPS) for 24 h. Both in FFP and supernatants, TNF, IL-1ß, IL-6, and IL-10 levels were measured by ELISA. Additionally, CD11B, TLR2, and CASP3 gene expression were measured by qtPCR in U937 cells. Total phagocytic activity was also assayed. RESULTS: Elevated IL-10, but low TNF and IL-1ß levels were measured in FFP from individuals aged 19-40 years, whereas in individuals aged 41-50 years FFP were characterized by equalized TNF and IL-10 levels. Elevated IL-6 levels were found in all FFP samples, especially in those from the oldest individuals. FFP stimulation was associated with striking modifications in cytokine production in an age-dependent way. Exposure to FFP attenuates the response to LPS. TLR2 and CD11B expression were enhanced regardless of the age of plasma donors, although CASP3 expression was increased only when FFP from individuals aged 19-40 years were tested. Phagocytosis decreased after exposure to FFP regardless of donor age. CONCLUSION: Our results suggest that soluble mediators in FFP may modulate the functioning of monocytes. Interestingly, this effect appears to be partially influenced by the age of donors.

Avaliação das subpopulações de monócitos em pacientes com tuberculose pulmonar / Evaluation of subpopulations of monocytes in patients with pulmonary tuberculosis

Os macrófagos são componentes importantes da resposta imune inata contra o Mycobaterium tuberculosis (Mtb) e podem desempenhar um papel importante na patogênese da tuberculose (TB). Macrófagos são derivados dos monócitos, os quais são classificados em subpopulações a partir da expressão da molécula de superfície CD14 e CD16. São denominados de clássicos, intermediários e não clássicos, e possuem diferenças funcionais e fenotípicas. Os fatores que levam ao desenvolvimento de TB ativa ainda não são claros. Um desequilíbrio entre subpopulações de monócitos circulantes pode estar envolvido na imunopatogênese da TB, uma vez que macrófagos são células importantes da resposta imune inicial da doença. Assim, neste estudo avaliou-se os subgrupos de monócitos em pacientes com TB ativa e latente (TBL). Voluntários com TB ativa, TBL e indivíduos saudáveis foram recrutados para avaliação de frequência, níveis de ativação e produção de citocinas dos subgrupos de monócitos circulantes e após a estimulação antigênica por citometria de fluxo. Nossos resultados não demonstraram diferenças significativas nas frequências, níveis de ativação e produções de citocinas das subpopulações de monócitos entre os grupos estudados. No entanto, pacientes com TB ativa tiveram um aumento na frequência dos monócitos clássicos ativados após estimulação antigênica comparados com os controles saudáveis. Não observou-se uma expansão das subpopulações CD16+ em pacientes TB. Por outro lado, se observou uma expansão dos monócitos CD16...

Macrophages are important components of the innate immune response against Mycobacterium tuberculosis (Mtb) and may play an important role in the pathogenesis of tuberculosis (TB). Macrophages are derived from monocytes, which are classified into subpopulations from the expression of CD14 and CD16 surface molecule. They are denominated classics, intermediate and non-classical, and have functional and phenotypic differences. The factors that lead to the development of active tuberculosis are not clear yet. However, an imbalance between subpopulations of monocytes may be involved in the immunopathogenesis of TB, since macrophages are important cells in the initial immune responses of the disease. In this study we evaluated the monocyte subsets in patients with active and latent TB (ILTB). Volunteers with active TB, ILTB and healthy subjects were recruited to evaluate the frequency, levels of activation and cytokine production of blood monocytes subsets circulating and after the antigenic stimulation by flow cytometry. Our results did not show significant differences in the frequency, activation levels and cytokine production of monocytes subsets between studies groups. However, patients with active TB have an increased of frequency and activated levels of classical monocytes after antigenic stimulation compared to healthy controls. An expansion of CD16+ in monocytes subsets of TB patient was not observed. Moreover, it was observed an expansion and increased activation of CD16...

Decreased phagocytic function in neutrophils and monocytes from peripheral blood in periodontal disease

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.

Stages of in vitro phagocytosis of Plasmodium falciparum-infected erythrocytes by human monocytes / Estágios da fagocitose in vitro por monócitos humanos de eritrócitos infectados por Plasmodium falciparum

Monocytes/macrophages play a critical role in the defense mechanisms against malaria parasites, and are the main cells responsible for the elimination of malaria parasites from the blood circulation. We carried out a microscope-aided evaluation of the stages of in vitro phagocytosis of Plasmodium falciparum-infected erythrocytes, by human monocytes. These cells were obtained from healthy adult individuals by means of centrifugation through a cushion of Percoll density medium and were incubated with erythrocytes infected with Plasmodium falciparum that had previously been incubated with a pool of anti-plasmodial immune serum. We described the stages of phagocytosis, starting from adherence of infected erythrocytes to the phagocyte membrane and ending with their destruction within the phagolisosomes of the monocytes. We observed that the different erythrocytic forms of the parasite were ingested by monocytes, and that the process of phagocytosis may be completed in around 30 minutes. Furthermore, we showed that phagocytosis may occur continuously, such that different phases of the process were observed in the same phagocyte.

Monócitos/macrófagos desempenham uma função crítica nos mecanismos de defesa antiplasmódio e constituem as principais células responsáveis pela eliminação das formas eritrocitárias do plasmódio da circulação sangüínea. Realizamos uma avaliação microscópica dos estágios da fagocitose in vitro de eritrócitos infectados por Plasmodium falciparum por monócitos humanos. Essas células foram obtidas de indivíduos adultos sadios por centrifugação em Percoll e incubadas com eritrócitos infectados por Plasmodium falciparum previamente incubados com um pool de soro imune contra plasmódio. Descrevemos os estágios da fagocitose, desde a aderência dos eritrócitos infectados até sua destruição nos fagolisossomas dos monócitos. Observou-se que eritrócitos infectados por todos os diferentes estágios assexuados do parasito foram ingeridos pelos monócitos e que o processo de fagocitose pode se completar em cerca de 30 minutos. Além disso, mostramos que a fagocitose pode ocorrer de uma forma contínua, de tal maneira que diferentes fases do processo foram observadas no mesmo fagócito.

Exercício abaixo do limiar anaeróbio aumenta as atividades fagocítica e microbicida de neutrófilos em ratos Wistar / Exercise below the anaerobic threshold increases phagocytic and microbicide activities of neutrophils in Wistar rats

OBJETIVO: Investigar o efeito de uma sessão de exercício abaixo do limiar anaeróbio sobre as funções de neutrófilos e monócitos circulantes em ratos Wistar. MATERIAL E MÉTODO: Trata-se de um delineamento experimental com um pós-teste em que os sujeitos do grupo experimental exercitaram-se na água por 30 minutos enquanto controles não foram submetidos a qualquer intervenção. A atividade funcional dos fagócitos circulantes foi avaliada por ensaio de fagocitose de Saccharomyces cerevisiae e pelo teste de redução de nitroazul de tetrazólio (NBT). Para comparação entre as médias dos grupos, utilizaram-se testes t para amostras independentes com p < 0,05. RESULTADO: Não foram observadas diferenças significativas no número total e diferencial de leucócitos entre os grupos. Entretanto, neutrófilos do grupo experimental não apenas fagocitaram mais S. cerevisiae (p = 0,005) como também foram mais eficientes em reduzir NBT (p = 0,018) em relação aos controles. Não existiram diferenças significativas na atividade funcional dos monócitos entre os grupos. CONCLUSÃO: O exercício realizado com intensidade abaixo do limiar anaeróbio foi suficiente para incrementar a atividade fagocítica e microbicida de neutrófilos em modelo animal, o mesmo não sendo observado para monócitos circulantes.

OBJECTIVE: To assess the effect of a single session of exercise conducted below the anaerobic threshold on the functions of neutrophils and circulating monocytes in Wistar rats. MATERIAL AND METHOD: This study had an experimental design with a single post-test in which subjects of the experimental group exercised in water for 30 minutes, whereas the control group was not submitted to any intervention. Functional capacity of circulating phagocytes was assessed by means of a phagocytosis assay of Saccharomyces cerevisiae and a nitro blue tetrazolium (NBT) reduction test. To compare means between groups, t tests for independent samples were used with p set at < 0.05. RESULTS: There were no significant differences as to the total and differential number of leucocytes between groups. Nonetheless, not only did the neutrophils of the experimental group phagocyte more S. cerevisiae (p = 0.005), but they also reduced NBT more efficiently (p = 0.018) in comparison with control subjects. No significant differences in these functional activities were observed in circulating monocytes. CONCLUSION: The exercise performed below the anaerobic threshold was sufficient to increase both phagocytic and microbicide activities of neutrophils in animal model, but the same protocol did not yield similar results for circulating monocytes.

Fagocitose e viabilidade monocitária de pacientes com esquistossomose mansônica na forma hepatoesplênica submetidos à esplenectomia e ao auto-implante esplênico / Phagocytes rate and cellular viability of the monocytes in patients with hepatosplenic schistosomiasis mansoni who underwent splenectomy and auto-implantation of spleen tissue

Esquistossomose mansônica persiste como problema médico-social no nordeste brasileiro. Em crianças, o tratamento cirúrgico inclui esplenectomia e auto-implante esplênico. Este procedimento reduz a septicemia pós-esplenectomia. O objetivo deste estudo foi analisar a taxa de fagocitose e viabilidade de fagócitos mononucleares em portadores de esquistossomose hepatoesplênica, submetidos à cirurgia, de 1991 a 2001. Dos 22 indivíduos analisados, 11 eram portadores de esquistossomose hepatoesplênica, submetidos à esplenectomia e auto-implante esplênico (Grupo estudo) e 11 eram sadios (Grupo Controle). Os grupos tinham média de idades similar e procediam da mesma zona endêmica (Timbaúba-PE). Não se evidenciou diferença na taxa de fagocitose comparando-se o grupo controle (36,1 por cento±4,9 por cento) e o grupo estudo (33,5 por cento±5,7 por cento), p=0,2773. Todavia, a viabilidade dos fagócitos após estímulo com lipopolissacarídio foi maior (94 por cento) no grupo controle, quando comparado ao grupo estudo (65 por cento), p<0,001. Pode-se concluir que a esplenose assegura função fagocitária normal em monócitos, entretanto, os fagócitos possuem menor viabilidade frente a um estímulo nocivo e duradouro.

Mansonic schistosomiasis remains a medical-social issue in Northeastern Brazil. In children, surgical treatment includes splenectomy and spleen autoimplantation. This procedure reduces post-splenectomy sepsis. The aim of this study was to analyze the phagocyte rate and the cellular viability of monocytes in patients with hepatosplenic schistosomiasis, who underwent splenectomy and spleen autoimplantation from 1991 to 2001. Of the 22 individuals analyzed, 11 were patients who underwent splenectomy and spleen autoimplantation (Study group) and 11 were healthy individuals from the same region (Control group). Both groups presented similar mean age. No difference was found in the phagocyte rate between the control group (36.1 percent±4.9 percent) and study group (33.5 percent±5.7 percent). However, phagocyte viability after stimulation with lipopolysaccharide was higher (94 percent) in control group, when compared to the study group (65 percent), p<0.001. It is possible to hypothesize that monocytes from the study group patients presented a reduced response to the microorganism challenge, in the face of a harmful and long-lasting stimulus.

Genetic potential for an acute inflammatory response in IgA glomerulonephritis in mice

Mice selected on the basis of an acute inflammatory response (AIR) can provide information about the immunopathological mechanisms of glomerulonephritis. We studied the differences between mice selected for a maximal AIR (AIRmax that attract more polymorphonuclear cells to the site of injury) or a minimal AIR (AIRmin that attract more mononuclear cells) in an experimental model of IgA nephropathy in order to investigate the effect of genetic background on glomerular disease progression and the participation of the monocyte chemoattractant protein-1 (MCP-1) chemokine. IgA nephropathy was induced by intraperitoneal ovalbumin injection and bile duct ligation in AIRmax and AIRmin mice. Histological changes, urinary protein/creatinine ratio, serum IgA levels, immunofluorescence for IgA, IgG and complement C3 fraction, immunohistochemistry for macrophages and MCP-1, and MCP-1 levels in macerated kidney were determined. Mesangial IgA deposition was seen only in AIRmin mice, which presented more renal lesions. Increased serum IgA levels (1.5 ± 0.4 vs 0.3 ± 0.1 mg/mL, P < 0.001), high glomerular MCP-1 expression and decreased monocyte/macrophage infiltration in the interstitial area (0.3 ± 0.3 vs 1.1 ± 0.9 macrophages/field, P < 0.05) were detected in AIRmin mice compared to AIRmax mice. No glomerular monocyte/macrophage infiltration was detected in either strain. In spite of the absence of IgA deposition, AIRmax mice presented discrete or absent mesangial proliferation. The study showed that there are differences between mice selected for AIRmax and AIRmin with respect to serum IgA levels, histological damage and MCP-1 chemokine production after ovalbumin injection in combination with bile duct ligation.

Phenotypic, functional, and quantitative characterization of canine peripheral blood monocyte-derived macrophages

The yield as well as phenotypic and functional parameters of canine peripheral blood monocyte-derived macrophages were analyzed. The cells that remained adherent to Teflon after 10 days of culture had high phagocytic activity when inoculated with Leishmania chagasi. Flow cytometric analysis demonstrated that more than 80 percent of cultured cells were positive for the monocyte/macrophage marker CD14.

Avaliação do efeito da esplenectomia e auto-implante esplênico sobre algumas funções de monócitos em crianças com esquistossomose mansônica / Evaluation of the effect of splenectomy with autologous spleen tissue implantation in some monocyte functions in children with hepatosplenic schistosomiasis mansoni

Investigamos em portadores de esquistossomose hepatoesplênica após esplenectomia com ou sem auto-implante esplênico: índice de aderência, produção de superóxido (SP) e de TNF-alfa em monócitos, tratados ou não com tuftsina. Avaliamos três grupos: voluntários sadios CG (grupo controle) (n=12); esplenectomizados com auto-implante AG (n=18) e esplenectomizados sem auto-implante WAG (n=9). índice de aderência e TNF-alfa não diferiram entre os grupos. SP foi semelhante em CG e AG na 1ª hora após estimulação celular. SP foi maior em todos intervalos de tempo nos grupos CG e AG, comparados ao WAG. O tratamento com tuftsina recuperou o padrão de normalidade de SP em AG, com aumento da 1ª para a 2ª hora nos níveis do CG. O tratamento com tuftsina não alterou SP em WAG, permanecendo reduzida em todos intervalos. O auto-implante esplênico parece recuperar e manter os parâmetros imunológicos avaliados, que têm participação importante na resposta do hospedeiro às infecções.

Increased Expression of Intracellular HLA-DM but Not on the Surface of Blood Monocyte-derived Dendritic Cells During Maturation

Cutaneous dendritic cells (DCs), Langerhans cells (LCs) and dermal dendritic cells (DDCs), are present in an immature state. The maturation of DCs is crucial for initiating an immune response. Since HLA-DM has an important role for antigen presentation, an increase in HLA-DM expression according to the maturation of blood monocyte-derived dendritic cells (MoDCs), which have similar characteristics with DDCs, is expected. Therefore, the aim of this study was to determine whether or not HLA-DM expression in MoDCs is related to maturation at each culture day (from day 0 to day 13) by flow cytometry. This was compared with the functional changes related to the maturation of MoDCs. MoDCs were generated by culturing human peripheral blood monocytes in the presence of GM-CSF and IL-4 for 7 days, which were followed by subsequent treatment with a cytokine cocktail (GM-CSF, IL-4, IL-1beta, TNF-alpha, IL-6 and PGE2) for the maturation of MoDCs. The intracellular HLA-DM was expressed in the immature MoDC. A sudden 3 to 8 fold increase in the intracellular HLA-DM expression was observed after treatment with a cytokine cocktail. HLA-DM was weakly expressed on the surface of the immature MoDC, but it seemed to be decreased with maturation. This study indicated that the intracellular HLA-DM expression increased, but not on the MoDC surface during maturation. This was despite the fact that HLA-DM expression was noted not only on the surface but also in the intracellular in the MoDC.

El caseinato de sodio induce la diferenciación de las células hematopoyéticas multipotenciales 32D / Sodium caseinate induces differentiation of the multipotential hemopoietic cell line 32D

Objetivo. Evaluar la participación del caseinato de sodio (CasNa) en la modulación de la hematopoyesis. Material y métodos. Se emplearon células 32D, una línea celular hematopoyética multipotencial, de origen murino y dependiente de interleucina-3. Estas células se cultivaron con 0.5 ng/mL de interleucina-3 y con concentraciones variables de CasNa. En los cultivos se realizaron estudios de proliferación celular (conteo directo e incorporación de timidina 3H) y de diferenciación morfológica (tinción con Giemsa), citoquímica (tinciones específicas para monocito-macrófagos y para granulocitos) y funcional (presencia de receptores Fc y reducción de nitro azul de tetrazolio), además se determinó la viabilidad con azul de tripano y la apoptosis por la reacción Tunel in situ. Resultados. Se demostró que el CasNa produce una reducción en la proliferación, dependiente de la dosis, que ésta no es provocada por una disminución de la viabilidad de las células 32D así como tampoco por un aumento de la muerte celular por apoptosis. Además el CasNa indujo la diferenciación de las células 32D hacia monocito-macrófagos en cultivos de 4 días. Conclusiones. Aparentemente el CasNa ejerce una actividad tipo factor estimulador de colonias de macrófagos. Además, parece ser un potente factor de diferenciación de las células 32D, ya que en sólo 4 días de estímulo genera células de tipo monocito-macrófago, a diferencia de los 7 días requeridos por la combinación de G-CSF y GM-CSF.

In vitro model of atherosclerosis using coculture of arterial wall cells and macrophage

In order to determine the precise mechanism of the interactions between different types of cells, which are common phenomena in tissues and organs, the importance of coculture techniques are becoming increasingly important. In the area of cardiology, artificial arteries have been developed, based on the understanding of physiological communication of the arterial smooth muscle cells (SMC), endothelial cells (EC), and the extracellular matrix (ECM). In the study of atherosclerosis, the modification of low-density lipoprotein (LDL), which result in the recruitment and accumulation of white blood cells, especially, monocytes/macrophages, and foam cell formation, are hypothesized. Although there are well known animal models, an in vitro model of atherogenesis with a precisely known atherogenesis mechanism has not yet been developed. In this paper, an arterial wall reconstruction model using rabbit primary cultivated aortic SMCs and ECs, was shown. In addition, human peripheral monocytes were used and the transmigration of monocytes was observed by scanning electron and laser confocal microscopy. Monocyte differentiation into macrophages was shown by immunohistochemistry and comprehensive gene expression analysis. With the modified form of LDL, the macrophages were observed to accumulate lipids with a foamy appearance and differentiate into the foam cells in the ECM between the ECs and SMCs in the area of our coculture model.

Interleukin 2 induction of proliferation in resting T lymphocytes requires contact with monocytes

Resting human T cells are known to express significant numbers of intermediate but none or barely detectable low and high a affinity IL-2 receptors (IL-2R). IL-2 alone failed to induce proliferation in these cells, However, in presence of small proportion of autologous monocytes, as low as 22 pM, IL-2 induced high levels of proliferation in resting T cells. Introduction of a semi permeable between the two cell types or addition of an anti-CD 11b mAb inhibited such induction of proliferation by IL-2. Neither recombinant IL-1 por IL-1 containing cell-free extracts from activated monocytes substituted for intact monocytes. Autologous B cells failed to replace monocytes. Using antigen-specific cloned human T cells we have shown a lack of requirement for antigen. The proliferation was inhibited by anti-IL-2R alpha mAb. IL-2 appears to be unique since neither IL-4 nor IL-6, alone or in presence of monocytes, led to induction of proliferation in resting T cells. Combination of IL-2 and monocytes induced proliferation in all T cell subpopulations (CD4, CD8, CD45RA and CD45RO) and antigen-specific clones examined. It also induces mRNA and surface expression of IL-2R alpha, appearance of high affinity IL-2R and induction of proliferation in large proportions of T cells. As in humans, the IL-2 induction of proliferation in murine resting T cell required contact with syngeneic monocytes, suggesting that such a mechanism of cells activation is highly conserved.

Factores genéticos del huésped en las enfermedades periodontales / Host genetic factors in periodontal diseases

Hasta tiempos recientes, la periodoncia estuvo orientada a determinar las noxas externas, lo que determinó un oscurecimiento de la participación de otros factores, tales como el genético. El objetivo del presente artículo es brindar al lector una visión de la combinación de la perspectiva molecular de la genética con la de la patogenia de las enfermedades periodontales

Senescent erythrocytes: modification of rheologic properties, antigenic expression and interaction with monocytes

Human erythrocytes have a well-defined lifespan of 120 days. Their eventual removal from circulation is a complex process affected by many cellular parameters, making them susceptible to sequestration in the spleen and other organs. The purpose of this study was to investigate putative changes in rheologic properties, antigenic expression and interaction with monocytes of senescent erythrocytes (SE). SE and young erythrocyte (YE) fractions were obtained by differential centrifugation from 20 healthy donor blood samples. Membrane rheomechanic properties (by difractometric method), ABO and MN antigens reactivity and erythrophagocytosis by peripheral monocytes were investigated in each fractions. SE showed a little decrease in the deformability index and an increase of both membrane elastic modulus and surface viscosity. The studies performed indicate a decreased expression in the antigens of both blood group systems studied (p < 0.01) and an increased rate of erythrophagocytosis by monocytes in SE compared to YE (p < 0.01). The significant modifications in the biomechanic properties of senescent red blood cell membrane and the loss antigenic expression could lead to physiological phagocytosis.

Macrófagos en el asma / Macrophages in asthma

Cada vez existen más demostraciones del papel que desempeña la línea monocito-macrófago en la patogénesis del asma bronquial. Las células fagocíticas mononucleares, como los macrófagos alveolares, también pueden activarse durante procesos alérgicos. Los monocitos macrófagos son posibles inductores potentes de la inflamación; ello debido a que pueden secretar mediadores inflamatorios, entre los que se cuentan los gránulos preformados de péptidos, metabolitos de activación de oxidación, factor activador de plaquetas y metabolitos del ácido araquidónico. La identificación de IL-1 en el liquido del lavado bronquial de enfermos asmáticos, así como la identificación de IL.1 en el líquido de ronchas de sitios de prueba de alergenos cutáneos, apoya el concepto de activación mononuclear de células fagociticas en padecimientos alérgicos

Evaluación de la actividad fagocitaria y bactericida de los monocitos y heterófilos aviares contra Samonella gallinarum / Evaluation of phagocytic and bactericidal activities of avian monocytes and heterophils against Salmonella gallinarum in vitro

Se determinó, mediante ensayos in vitro, la capacidad fagocítica y bactericida de los deterófilos y de los monocitos aviares contra Salmonella gallinarum, en presencia y en ausencia de 10 por ciento de suero hiperinmune. En los ensayos de fagocitosis se observó que los hetrófilos fagocitaron al 28 ñ 4.7 por ciento de las bacterias sin opsonizar y al 45 ñ 9.9 por ciento de las bacterias opsonizadas, obteniéndose diferencias significativas (P< 0.05). En contraste, los monocitos sólo fagocitaron un 10.3 ñ 4.2 por ciento y un 11.7 ñ 3.8 por ciento de bacterias opsonizadas y sin opsonizar respectivamente (P> 0.05). En los ensayos bactericidas se observó que los heterófilos destruyeron al 90.46 ñ 3.3 por ciento de la bacteria sin opsonizar y 90 ñ 2.3 por ciento de la bacteria opsonizada (P> 0.05); sin embargo, en los monocitos se obtuvo un 10.5 ñ 6.6 por ciento y un 84.74 ñ 5 por ciento respectivamante, obteniéndose diferencias significativas (P< 0.05). Los resultados del presente estudio indican que la fagocitosis de los heterófilos fue significativamente incrementada por la opsonización; en el caso de los monocitos, no hubo un efecto significativamente mayor. Aproximadamente el 90 por ciento de las bacterias fagocitadas por los heterófilos fueron destruidos, como se determinó en el ensayo. La opsonización no incrementó significativamante el porcentaje de bacteria destruida por parte de los heterófilos, sin embargo, la psonización de Salmonella gallinarum sí favoreció la capacidad bactericida de los monocitos

Impaired monocyte function in patients succesfully treated for Wipple's disease

Peripheral blood mononuclear cells (monocytes) from patients with Whipple's disease in long-term remission were tested for their ability to handle intracellular microorganisms. Phagocytosis and lysis of Candida tropicalis by monocytes of patients (n=12) andcontrols (n=8) were quantified after 30 min of incubation. Phagocytosis was similar in both groups but intracellular Killing of Candida tropicalis was significativily lower in patients (p<0.001). We concluded that our study showed an in vitro defect in the intracellular Killing function of monocytes in subjects in remission many years after diagnosis of Whipple's disease. The defective function did not seem to be related to relapse or to the susceptibility to other infections.