RESUMEN
CD4+ T cell-mediated immunity against Streptococcus pneumoniae (pneumococcus) can protect against recurrent bacterial colonization and invasive pneumococcal diseases (IPDs). Although such immune responses are common, the pertinent antigens have remained elusive. We identified an immunodominant CD4+ T cell epitope derived from pneumolysin (Ply), a member of the bacterial cholesterol-dependent cytolysins (CDCs). This epitope was broadly immunogenic as a consequence of presentation by the pervasive human leukocyte antigen (HLA) allotypes DPB1∗02 and DPB1∗04 and recognition via architecturally diverse T cell receptors (TCRs). Moreover, the immunogenicity of Ply427-444 was underpinned by core residues in the conserved undecapeptide region (ECTGLAWEWWR), enabling cross-recognition of heterologous bacterial pathogens expressing CDCs. Molecular studies further showed that HLA-DP4-Ply427-441 was engaged similarly by private and public TCRs. Collectively, these findings reveal the mechanistic determinants of near-global immune focusing on a trans-phyla bacterial epitope, which could inform ancillary strategies to combat various life-threatening infectious diseases, including IPDs.
Asunto(s)
Linfocitos T CD4-Positivos , Citotoxinas , Humanos , Bacterias , Epítopos de Linfocito T , ColesterolRESUMEN
Introducción: La artritis reumatoide es una enfermedad autoinmune sistémica, aunque afecta fundamentalmente las articulaciones sinoviales. Más allá de las implicaciones para la calidad de vida del paciente, la presencia de la artritis reumatoide se asocia con una reducción de la esperanza de vida entre 5-10 años. La tasa de mortalidad estandarizada asociada a la artritis reumatoide es superior a la encontrada en la población no afectada; y este exceso de mortalidad se atribuye en gran medida a las enfermedades cardiovasculares, de las cuales la enfermedad vascular aterosclerótica es su principal componente. Objetivo: Determinar cómo se comportaron los factores de riesgo de enfermedad cardiovascular aterosclerótica en pacientes con diagnóstico de artritis reumatoide comparado con el grupo control. Métodos: Se realizó un estudio observacional, de tipo caso-control durante el período comprendido entre enero de 2007 y enero de 2017. Se estudiaron 110 pacientes y 220 controles. En ambos grupos se analizó la frecuencia de factores de riesgo de enfermedad cardiovascular aterosclerótica (tabaquismo, hipertensión arterial, diabetes mellitus y dislipidemia), machados por edad y sexo. Resultados: Predominaron los pacientes del sexo femenino. La mediana de edad de los pacientes fue de 41,0 años. El tabaquismo fue más frecuente en los casos (23,6 por ciento vs 11,4 por ciento, p=0,004), así como la hipertensión arterial y la diabetes mellitus. Conclusiones: En el presente estudio los factores de riesgo como el tabaquismo, la diabetes mellitus y la dislipidemia fueron más frecuentes en los pacientes son artritis reumatoide que en el grupo control(AU)
Introduction: Rheumatoid arthritis is a systemic autoimmune disease, although it mainly affects the synovial joints. Beyond the implications for the patient's quality of life, the presence of rheumatoid arthritis is associated with a reduction in life expectancy in 5-10 years. The standardized mortality rate associated with rheumatoid arthritis is higher than that found in the unaffected population; and this excess mortality is largely attributed to cardiovascular diseases, of which atherosclerotic vascular disease is the main component. Objective: To determine how the risk factors for atherosclerotic cardiovascular disease behaved in patients diagnosed with rheumatoid arthritis compared to the control group. Methods: An observational, case-control study was carried out from January 2007 to January 2017. A hundred ten (110) patients and 220 controls were studied. In both groups, the frequency of risk factors for atherosclerotic cardiovascular disease (smoking, high blood pressure, diabetes mellitus, and dyslipidemia) was analyzed, matched by age and sex. Results: Female patients predominated. The median age of the patients was 41.0 years. Smoking was more frequent variable in the cases (23.6percent vs 11.4percent, p=0.004), as well as arterial hypertension and diabetes mellitus. Conclusions: In the present study, risk factors such as smoking, diabetes mellitus and dyslipidemia were more frequent in patients with rheumatoid arthritis than in the control group(AU)
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Humanos , Masculino , Femenino , Factores de Riesgo de Enfermedad Cardiaca , Estudio ObservacionalRESUMEN
Antibodies specific for peptides bound to human leukocyte antigen (HLA) molecules are valuable tools for studies of antigen presentation and may have therapeutic potential. Here, we generated human T cell receptor (TCR)-like antibodies toward the immunodominant signature gluten epitope DQ2.5-glia-α2 in celiac disease (CeD). Phage display selection combined with secondary targeted engineering was used to obtain highly specific antibodies with picomolar affinity. The crystal structure of a Fab fragment of the lead antibody 3.C11 in complex with HLA-DQ2.5:DQ2.5-glia-α2 revealed a binding geometry and interaction mode highly similar to prototypic TCRs specific for the same complex. Assessment of CeD biopsy material confirmed disease specificity and reinforced the notion that abundant plasma cells present antigen in the inflamed CeD gut. Furthermore, 3.C11 specifically inhibited activation and proliferation of gluten-specific CD4+ T cells in vitro and in HLA-DQ2.5 humanized mice, suggesting a potential for targeted intervention without compromising systemic immunity.
Asunto(s)
Linfocitos T CD4-Positivos/inmunología , Enfermedad Celíaca/inmunología , Glútenes/inmunología , Antígenos HLA-DQ/inmunología , Péptidos/inmunología , Receptores de Antígenos de Linfocitos T/inmunología , Animales , Línea Celular Tumoral , Epítopos de Linfocito T/inmunología , Glútenes/química , Antígenos HLA-DQ/química , Humanos , Activación de Linfocitos/inmunología , Ratones , Modelos Moleculares , Péptidos/química , Receptores de Antígenos de Linfocitos T/químicaRESUMEN
DEC-205 (CD205), a member of the macrophage mannose receptor protein family, is the prototypic endocytic receptor of dendritic cells, whose ligands include phosphorothioated cytosine-guanosine oligonucleotides, a motif often seen in bacterial or viral DNA. However, despite growing biological and clinical significance, little is known about the structural arrangement of this receptor or any of its family members. Here, we describe the 3.2 Å cryo-EM structure of human DEC-205, thereby illuminating the structure of the mannose receptor protein family. The DEC-205 monomer forms a compact structure comprising two intercalated rings of C-type lectin-like domains, where the N-terminal cysteine-rich and fibronectin domains reside at the central intersection. We establish a pH-dependent oligomerization pathway forming tetrameric DEC-205 using solution-based techniques and ultimately solved the 4.9 Å cryo-EM structure of the DEC-205 tetramer to identify the unfurling of the second lectin ring which enables tetramer formation. Furthermore, we suggest the relevance of this oligomerization pathway within a cellular setting, whereby cytosine-guanosine binding appeared to disrupt this cell-surface oligomer. Accordingly, we provide insight into the structure and oligomeric assembly of the DEC-205 receptor.
Asunto(s)
Antígenos CD/química , Antígenos CD/metabolismo , Microscopía por Crioelectrón/métodos , Fibronectinas/metabolismo , Lectinas Tipo C/metabolismo , Antígenos de Histocompatibilidad Menor/química , Antígenos de Histocompatibilidad Menor/metabolismo , Receptores de Superficie Celular/química , Receptores de Superficie Celular/metabolismo , Humanos , Lectinas Tipo C/química , Ligandos , Conformación ProteicaRESUMEN
The transmembrane metalloprotease ADAM10 sheds a range of cell surface proteins, including ligands and receptors of the Notch, Eph, and erbB families, thereby activating signaling pathways critical for tumor initiation and maintenance. ADAM10 is thus a promising therapeutic target. Although widely expressed, its activity is normally tightly regulated. We now report prevalence of an active form of ADAM10 in tumors compared with normal tissues, in mouse models and humans, identified by our conformation-specific antibody mAb 8C7. Structure/function experiments indicate mAb 8C7 binds an active conformation dependent on disulfide isomerization and oxidative conditions, common in tumors. Moreover, this active ADAM10 form marks cancer stem-like cells with active Notch signaling, known to mediate chemoresistance. Importantly, specific targeting of active ADAM10 with 8C7 inhibits Notch activity and tumor growth in mouse models, particularly regrowth after chemotherapy. Our results indicate targeted inhibition of active ADAM10 as a potential therapy for ADAM10-dependent tumor development and drug resistance.
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Proteína ADAM10/fisiología , Neoplasias Experimentales/patología , Células Madre Neoplásicas/patología , Proteína ADAM10/antagonistas & inhibidores , Proteína ADAM10/química , Proteína ADAM17/fisiología , Secuencias de Aminoácidos , Animales , Anticuerpos Monoclonales/química , Anticuerpos Monoclonales/inmunología , Humanos , Masculino , Ratones , Ratones Endogámicos BALB C , Receptores Notch/fisiologíaRESUMEN
Eph receptors and their corresponding membrane-bound ephrin ligands regulate cell positioning and establish tissue patterns during embryonic and oncogenic development. Emerging evidence suggests that assembly of polymeric Eph signalling clusters relies on cytoskeletal reorganisation and underlies regulation by protein tyrosine phosphatases (PTPs). PTP-PEST (also known as PTPN12) is a central regulator of actin cytoskeletal dynamics. Here, we demonstrate that an N-terminal fragment of PTP-PEST, generated through an ephrinA5-triggered and spatially confined cleavage mediated by caspase-3, attenuates EphA3 receptor activation and its internalisation. Isolation of EphA3 receptor signalling clusters within intact plasma membrane fragments obtained by detergent-free cell fractionation reveals that stimulation of cells with ephrin triggers effective recruitment of this catalytically active truncated form of PTP-PEST together with key cytoskeletal and focal adhesion proteins. Importantly, modulation of actin polymerisation using pharmacological and dominant-negative approaches affects EphA3 phosphorylation in a similar manner to overexpression of PTP-PEST. We conclude that PTP-PEST regulates EphA3 activation both by affecting cytoskeletal remodelling and through its direct action as a PTP controlling EphA3 phosphorylation, indicating its multifaceted regulation of Eph signalling.
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Efrina-A5/fisiología , Proteína Tirosina Fosfatasa no Receptora Tipo 12/fisiología , Proteínas Tirosina Quinasas Receptoras/metabolismo , Animales , Células COS , Caspasa 3/metabolismo , Membrana Celular/metabolismo , Chlorocebus aethiops , Citoesqueleto/metabolismo , Células HEK293 , Humanos , Fosforilación , Unión Proteica , Procesamiento Proteico-Postraduccional , Transporte de Proteínas , Receptor EphA3RESUMEN
Eph and ephrin proteins are essential cell guidance cues that orchestrate cell navigation and control cell-cell interactions during developmental tissue patterning, organogenesis and vasculogenesis. They have been extensively studied in animal models of embryogenesis and adult tissue regeneration, but less is known about their expression and function during human tissue and organ regeneration. We discovered the hypoxia inducible factor (HIF)-1α-controlled expression of EphA3, an Eph family member with critical functions during human tumour progression, in the vascularised tissue of regenerating human endometrium and on isolated human endometrial multipotent mesenchymal stromal cells (eMSCs), but not in other highly vascularised human organs. EphA3 affinity-isolation from human biopsy tissue yielded multipotent CD29+/CD73+/CD90+/CD146+ eMSCs that can be clonally propagated and respond to EphA3 agonists with EphA3 phosphorylation, cell contraction, cell-cell segregation and directed cell migration. EphA3 silencing significantly inhibited the ability of transplanted eMSCs to support neovascularisation in immunocompromised mice. In accord with established roles of Eph receptors in mediating interactions between endothelial and perivascular stromal cells during mouse development, our findings suggest that HIF-1α-controlled expression of EphA3 on human MSCs functions during the hypoxia-initiated early stages of adult blood vessel formation.
Asunto(s)
Células Madre Mesenquimatosas/metabolismo , Células Madre Multipotentes/metabolismo , Neovascularización Fisiológica , Receptor EphA3/genética , Adulto , Animales , Western Blotting , Hipoxia de la Célula , Células Cultivadas , Endometrio/citología , Femenino , Expresión Génica , Xenoinjertos/irrigación sanguínea , Humanos , Subunidad alfa del Factor 1 Inducible por Hipoxia/genética , Subunidad alfa del Factor 1 Inducible por Hipoxia/metabolismo , Masculino , Trasplante de Células Madre Mesenquimatosas/métodos , Ratones Endogámicos BALB C , Ratones Desnudos , Microscopía Fluorescente , Células Madre Multipotentes/trasplante , Interferencia de ARN , Receptor EphA3/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Trasplante Heterólogo , Adulto JovenRESUMEN
Eph receptor tyrosine kinases are critical for cell-cell communication during normal and oncogenic tissue patterning and tumor growth. Somatic mutation profiles of several cancer genomes suggest EphA3 as a tumor suppressor, but its oncogenic expression pattern and role in tumorigenesis remain largely undefined. Here, we report unexpected EphA3 overexpression within the microenvironment of a range of human cancers and mouse tumor xenografts where its activation inhibits tumor growth. EphA3 is found on mouse bone marrow-derived cells with mesenchymal and myeloid phenotypes, and activation of EphA3(+)/CD90(+)/Sca1(+) mesenchymal/stromal cells with an EphA3 agonist leads to cell contraction, cell-cell segregation, and apoptosis. Treatment of mice with an agonistic α-EphA3 antibody inhibits tumor growth by severely disrupting the integrity and function of newly formed tumor stroma and microvasculature. Our data define EphA3 as a novel target for selective ablation of the tumor microenvironment and demonstrate the potential of EphA3 agonists for anticancer therapy.
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Anticuerpos Monoclonales/farmacología , Proteínas Tirosina Quinasas Receptoras/agonistas , Proteínas Tirosina Quinasas Receptoras/biosíntesis , Receptor EphA3/agonistas , Receptor EphA3/biosíntesis , Animales , Apoptosis/efectos de los fármacos , Línea Celular Tumoral , Transformación Celular Neoplásica , Modelos Animales de Enfermedad , Regulación Neoplásica de la Expresión Génica , Células HEK293 , Humanos , Ratones , Ratones Desnudos , Terapia Molecular Dirigida , Proteínas Tirosina Quinasas Receptoras/inmunología , Proteínas Tirosina Quinasas Receptoras/metabolismo , Receptor EphA3/inmunología , Receptor EphA3/metabolismo , Transducción de Señal , Células del Estroma/efectos de los fármacos , Células del Estroma/patología , Microambiente Tumoral/efectos de los fármacosRESUMEN
Introducción: la prueba de VDRL (venereal disease research laboratories) es una técnica no treponémica de microfloculación en lámina para la detección cualitativa y semicuantitativa de reaginas plasmáticas. El VDRL Plus es un juego de reactivos que contiene una suspensión antigénica estabilizada (no alcohólica), basada en una mezcla de cardiolipina, colesterol y lecitina en tampón fosfato. Objetivo: determinar un conjunto de parámetros funcionales que caracterizan el desempeño diagnóstico o clínico del juego de reactivo VDRL Plus producido en Centro de Isótopos (CENTIS). Métodos: los parámetros del desempeño diagnóstico evaluados fueron: sensibilidad y especificidad diagnóstica, valores predictivos positivo y negativo, razón de verosimilitud positiva y negativa. Se determinaron además los índices de Youden y de concordancia Kappa. Se emplearon como métodos de referencia TPHA (Treponema pallidum hemagglutination) y RPR (rapid plasma reagin)-carbón producidos en el CENTIS. Se utilizaron muestras de sueros obtenidas en diferentes instituciones de salud de La Habana y el estudio se realizó con dos lotes del producto. Resultados: para los dos lotes evaluados se obtuvieron valores de sensibilidad de 100 porciento y de especificidad diagnóstica de 81 y 84 porciento. Los valores predictivos positivos resultaron de 71 y 75 porciento, y los negativos de 100 porciento. Por su parte, las razones de verosimilitud negativas fueron de 0 porciento y las positivas de 5,3 y 6,3 porciento, para cada lote estudiado. Los índices de Youden obtenidos (0,84 y 0,81) y la concordancia expresada mediante Kappa muestran que existe una adecuada correlación entre los resultados con el método en evaluación y los de referencia. Conclusiones: las características funcionales evaluadas evidencian que el diagnosticador VDRL Plus es apto para el uso previsto y que estas son consistentes entre los lotes estudiados
Introduction: the VDRL test (venereal disease research laboratories) is a no-treponemal slide microaglutination test for the qualitative and semi-quantitative detection of plasma reagins in human serum. The VDRL Plus contains non alcoholic stabilized antigen suspension based in cardiolipin, lecithin and cholesterol in phosphate buffer. Objective: to determine a group of functional parameters in the diagnostic or clinical performance of the VDRL Plus set of reagents produced by the Center of Isotopes (CENTIS). Methods: several parameters, such as, sensitivity, specificity, positive and negative predictive values and positive and negative likelihood ratios were evaluated. Likewised, Youden and Kappa indexes were calculated. Two references methods were employed, that is, TPHA (Treponema pallidum hemagglutination) and RPR-Carbon (rapid plasma reagin)-carbon, both from CENTIS. Serum samples were collected from several health centers in Havana city. Two different product batches were evaluated. Results: the sensitivity value for both evaluated batches was 100 percent and the specificity was 81 and 84 percent. The positives predictive values were 71 and 75 percent and negative predictive value was 100 percent. The positive likelihood ration were 5.3 and 6,3 percent respectively and negative likelihood ration was 0 percent for both batches. The Youden indexes obtained (0.84 and 0.81) and Kappa's indexes showed that there was an adequate correlation between the results obtained and the evaluation and reference methods. Conclusions: the evaluated functional characteristics showed that they are consistent among studied batches and that the VDRL Plus assay is suitable for the intended use
Asunto(s)
Humanos , Masculino , Femenino , Enfermedades Bacterianas de Transmisión Sexual/microbiología , Indicadores y Reactivos/análisis , Juego de Reactivos para Diagnóstico/microbiología , Sensibilidad y Especificidad , Técnicas de Laboratorio Clínico/métodosRESUMEN
Introducción: la prueba de VDRL (venereal disease research laboratories) es una técnica no treponémica de microfloculación en lámina para la detección cualitativa y semicuantitativa de reaginas plasmáticas. El VDRL Plus es un juego de reactivos que contiene una suspensión antigénica estabilizada (no alcohólica), basada en una mezcla de cardiolipina, colesterol y lecitina en tampón fosfato. Objetivo: determinar un conjunto de parámetros funcionales que caracterizan el desempeño diagnóstico o clínico del juego de reactivo VDRL Plus producido en Centro de Isótopos (CENTIS). Métodos: los parámetros del desempeño diagnóstico evaluados fueron: sensibilidad y especificidad diagnóstica, valores predictivos positivo y negativo, razón de verosimilitud positiva y negativa. Se determinaron además los índices de Youden y de concordancia Kappa. Se emplearon como métodos de referencia TPHA (Treponema pallidum hemagglutination) y RPR (rapid plasma reagin)-carbón producidos en el CENTIS. Se utilizaron muestras de sueros obtenidas en diferentes instituciones de salud de La Habana y el estudio se realizó con dos lotes del producto. Resultados: para los dos lotes evaluados se obtuvieron valores de sensibilidad de 100 porciento y de especificidad diagnóstica de 81 y 84 porciento. Los valores predictivos positivos resultaron de 71 y 75 porciento, y los negativos de 100 porciento. Por su parte, las razones de verosimilitud negativas fueron de 0 porciento y las positivas de 5,3 y 6,3 porciento, para cada lote estudiado. Los índices de Youden obtenidos (0,84 y 0,81) y la concordancia expresada mediante Kappa muestran que existe una adecuada correlación entre los resultados con el método en evaluación y los de referencia. Conclusiones: las características funcionales evaluadas evidencian que el diagnosticador VDRL Plus es apto para el uso previsto y que estas son consistentes entre los lotes estudiados(AU)
Introduction: the VDRL test (venereal disease research laboratories) is a no-treponemal slide microaglutination test for the qualitative and semi-quantitative detection of plasma reagins in human serum. The VDRL Plus contains non alcoholic stabilized antigen suspension based in cardiolipin, lecithin and cholesterol in phosphate buffer. Objective: to determine a group of functional parameters in the diagnostic or clinical performance of the VDRL Plus set of reagents produced by the Center of Isotopes (CENTIS). Methods: several parameters, such as, sensitivity, specificity, positive and negative predictive values and positive and negative likelihood ratios were evaluated. Likewised, Youden and Kappa indexes were calculated. Two references methods were employed, that is, TPHA (Treponema pallidum hemagglutination) and RPR-Carbon (rapid plasma reagin)-carbon, both from CENTIS. Serum samples were collected from several health centers in Havana city. Two different product batches were evaluated. Results: the sensitivity value for both evaluated batches was 100 percent and the specificity was 81 and 84 percent. The positives predictive values were 71 and 75 percent and negative predictive value was 100 percent. The positive likelihood ration were 5.3 and 6,3 percent respectively and negative likelihood ration was 0 percent for both batches. The Youden indexes obtained (0.84 and 0.81) and Kappa's indexes showed that there was an adequate correlation between the results obtained and the evaluation and reference methods. Conclusions: the evaluated functional characteristics showed that they are consistent among studied batches and that the VDRL Plus assay is suitable for the intended use(AU)
Asunto(s)
Humanos , Masculino , Femenino , Indicadores y Reactivos/análisis , Enfermedades Bacterianas de Transmisión Sexual/microbiología , Juego de Reactivos para Diagnóstico/microbiología , Técnicas de Laboratorio Clínico/métodos , Sensibilidad y EspecificidadRESUMEN
The ADAM10 transmembrane metalloprotease cleaves a variety of cell surface proteins that are important in disease, including ligands for receptor tyrosine kinases of the erbB and Eph families. ADAM10-mediated cleavage of ephrins, the ligands for Eph receptors, is suggested to control Eph/ephrin-mediated cell-cell adhesion and segregation, important during normal developmental processes, and implicated in tumour neo-angiogenesis and metastasis. We previously identified a substrate-binding pocket in the ADAM10 C domain that binds the EphA/ephrin-A complex thereby regulating ephrin cleavage. We have now generated monoclonal antibodies specifically recognising this region of ADAM10, which inhibit ephrin cleavage and Eph/ephrin-mediated cell function, including ephrin-induced Eph receptor internalisation, phosphorylation and Eph-mediated cell segregation. Our studies confirm the important role of ADAM10 in cell-cell interactions mediated by both A- and B-type Eph receptors, and suggest antibodies against the ADAM10 substrate-recognition pocket as promising therapeutic agents, acting by inhibiting cleavage of ephrins and potentially other ADAM10 substrates.
Asunto(s)
Proteínas ADAM/metabolismo , Anticuerpos Monoclonales/metabolismo , Efrinas/metabolismo , Receptores de la Familia Eph/metabolismo , Proteínas ADAM/genética , Proteínas ADAM/inmunología , Animales , Anticuerpos Monoclonales/genética , Anticuerpos Monoclonales/inmunología , Sitios de Unión de Anticuerpos , Bovinos , Adhesión Celular , Células HEK293 , Humanos , Ratones , Unión Proteica , Transducción de SeñalRESUMEN
Se evaluó un método de aglutinación con látex para la detección de proteína C reactiva (PCR) (PCR-Látex, CENTIS) empleándose como referencia un test turbidimétrico (PCR-Turbilátex, Spinreact). Se procesaron en paralelo 97 sueros de pacientes con clínica sugestiva de inflamación y sepsis. El análisis estadístico incluyó la determinación de la sensibilidad, especificidad, valor predictivo positivo (VPP), valor predictivo negativo (VPN) y límites de detección. Los resultados obtenidos de sensibilidad: 97,8 %; especificidad: 98,0 %; VPP: 97,8 %; VPN: 98,0 %, con un límite de detección de 6 mg/L, pueden considerarse de satisfactorios, lo que permite contar con un procedimiento sencillo, rápido y eficiente que no requiere de un equipamiento especial.
Agglutination evaluation method related to use of latex for detection of reactive C protein (RCP) (RCP-Latex, CENTIS) was evaluated, using as reference a turbidimetry test (RCP-Turbilatex, Spinreact). In parallel, 97 sera from patients with possibilities of inflammation and sepsis were processed. Statistical analysis included determination of sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and detection limits. Results achieved for sensitivity: 97,8 %; specificity: 98,0 %; NVP: 97,8 %; NPV: 98 % with a detection limit of 6 mg/L, may be considered of satisfactory, allowing to have a simple, fast, and efficient procedure without a especial equipment.
RESUMEN
Se evaluó un método de aglutinación con látex para la detección de proteína C reactiva (PCR) (PCR-Lßtex, CENTIS) empleándose como referencia un test turbidimétrico (PCR-Turbilátex, Spinreact). Se procesaron en paralelo 97 sueros de pacientes con clínica sugestiva de inflamación y sepsis. El análisis estadístico incluyó la determinación de la sensibilidad, especificidad, valor predictivo positivo (VPP), valor predictivo negativo (VPN) y límites de detección. Los resultados obtenidos de sensibilidad: 97,8 por ciento; especificidad: 98,0 por ciento; VPP: 97,8 por ciento; VPN: 98,0 por ciento, con un límite de detección de 6 mg/L, pueden considerarse de satisfactorios, lo que permite contar con un procedimiento sencillo, rápido y eficiente que no requiere de un equipamiento especial(AU)
Agglutination evaluation method related to use of latex for detection of reactive C protein (RCP) (RCP-Latex, CENTIS) was evaluated, using as reference a turbidimetry test (RCP-Turbilatex, Spinreact). In parallel, 97 sera from patients with possibilities of inflammation and sepsis were processed. Statistical analysis included determination of sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and detection limits. Results achieved for sensitivity: 97,8 percent; specificity: 98,0 percent; NVP: 97,8 percent; NPV: 98 percent with a detection limit of 6 mg/L, may be considered of satisfactory, allowing to have a simple, fast, and efficient procedure without a especial equipment(AU)