Laboratory testing techniques for monkeypox virus / 中华皮肤科杂志

Monkeypox is a zoonotic viral disease caused by monkeypox virus infection. Monkeypox has become a public health emergency of international concern, since it first spread widely in many regions outside Africa in 2022. Accurate and effective detection methods are particularly important for the diagnosis and screening of monkeypox virus infection. This review summarizes laboratory testing techniques for monkeypox virus in recent years, and compares principles and detection performance of microscopy, culture, nucleic acid testing and immunological methods.

Metaanálisis de la validez del inmunodiagnóstico del virus linfotrópico de células T humanas i/ii en bancos de sangre, 2000-2018 / Meta-analysis regarding the validity of the immunodiagnosis of human T-cell lymphotropic virus I/II in blood banks, 2000-2018 / Meta-análise da validade do imunodiagnóstico do vírus linfotrópico de células t humanas I/II em bancos de sangue, 2000-2018

Resumen Objetivo: Evaluar la validez del inmunodiagnóstico del htlv i/ii en bancos de sangre, con base en estudios publicados en la literatura científica. Metodología: Se efectuó un metaanálisis de pruebas diagnósticas siguiendo la guía prisma y las recomendaciones de Cochrane. Se evaluó la calidad metodológica con quadas y se garantizó la reproducibilidad y la exhaustividad. Se realizó también un análisis de efectos aleatorios para la sensibilidad, la especificidad, los cocientes de probabilidad, la razón de momios diagnóstica y la curva característica operativa del receptor (roc) con sus intervalos de confianza (ic) del 95 %. Resultados: Se tamizaron 4604 estudios, de los cuales solo tres cumplieron el protocolo. Se evaluaron 548 infectados con htlv i/ii y 6643 sanos. El inmunodiagnóstico de htlv i/ii presentó una sensibilidad del 99 % (ic95 % = 98,0-99,0), especificidad del 100 % (ic95 % = 99,9-100), cocientes de probabilidad positivo de 315,8 (ic95 % = 128,2-778,5) y negativo de 0,02 (ic95 % = 0,01-0,04), razón de momios diagnóstica de 24373 (ic95 % = 6864-86545) y área bajo la curva roc del 99,9 %. Conclusión: Se dispone de pocos estudios en este campo del inmunodiagnóstico htlv i/ii. El elevado número de sujetos analizados evidenció alta validez del inmunodiagnóstico, lo que resulta determinante para garantizar la inocuidad de las unidades de sangre, la detección de portadores asintomáticos, la disminución de la transmisión y el inicio de tratamiento.

Abstract Objective: To evaluate the validity of the immunodiagnosis of htlv i/ii in blood banks, based on studies published in the scientific literature. Methodology: A meta-analysis of diagnostic tests was carried out following the PRISMA guidelines and Cochrane recommendations. The methodological quality was evaluated with QUADAS, and reproducibility and completeness were guaranteed. A random effects analysis was also performed with respect to sensitivity, specificity, likelihood ratios, diagnostic odds ratio, and receiver operating characteristic curve (ROC) with their 95 % confidence intervals (CI). Results: 4,604 studies were screened, of which only three complied with the protocol. 548 subjects infected with HTLV I/II and 6,643 healthy subjects were evaluated. The immunodiagnosis of HTLV I/II had a sensitivity of 99 % (95 % CI = 98.0-99.0), a specificity of 100 % (95 % CI = 99.9-100), a positive likelihood ratio of 315.8 (95 % CI = 128.2-778.5) and a negative likelihood ratio of 0.02 (95 % CI = 0.01-0.04), a diagnostic odds ratio of 24,373 (95 % CI = 6,864-86,545), and an area under the ROC curve of 99.9 %. Conclusion: Few studies are available in the field of HTLV I/II immunodiagnosis. The high number of subjects analyzed showed high validity of the immunodiagnosis, which is decisive to guarantee the safety of the blood units, the detection of asymptomatic carriers, the decrease in transmission, and the start of treatment.

Resumo Objetivo: Avaliar a validade do imunodiagnóstico do HTLV I/II nos bancos de sangue, baseados nos estudos publicados na literatura científica. Metodologia: Foi realizada uma meta-análise de testes diagnósticos seguindo a guia PRISMA e as recomendações de Cochrane. Foi avaliada a qualidade metodológica com QUADAS e garantiu-se a reprodutibilidade e a integridade. Realizou-se também uma análise de efeitos aleatórios para a sensibilidade, a especificidade, os quocientes de probabilidade, a razão de probabilidade diagnóstica e a Curva Característica de Operação do Receptor (Curva ROC) com seus Intervalos de Confiança (IC) de 95%. Resultados: Foram selecionados 4604 estudos, dos quais somente 3 cumpriram com o protocolo. Foram avaliados 548 infectados com o vírus HTLV I/II e 6.643 saudáveis. O imunodiagnóstico de HTLV I/II apresentou uma sensibilidade de 99% (IC95% = 98,0-99,0), especificidade de 100% (IC95%= 99,9-100), quocientes de probalidade positiva de 315,8 (IC95% = 128,2-778,5) e negativo de 0,02 (IC95% = 0,01-0,04), razão de probabilidade diagnóstica de 24373 (IC95% = 6864-86545) e área sob a curva ROC de 99,9%. Conclusão: São poucos os estudos disponíveis neste campo do imunodiagnóstico HTLV I/II. O elevado número de pessoas analisadas evidenciou alta validade do imunodiagnóstico, o que é decisivo para garantir a inocuidade das unidades de sangue, a detecção de portadores assintomáticos, a diminuição da transmissão e o início do tratamento.

Seroprevalence of Hepatitis C Virus in a blood bank of Medellín-Colombia, 2005-2018 / Seroprevalencia del virus de la hepatitis c en un banco de sangre de medellín-colombia, 2005-2018

RESUMEN El objetivo de este estudio fue estimar la seroprevalencia del virus de la hepatitis C (VHC) en donantes de un banco de sangre de Medellín- Colombia en el periodo 2005-2018 e identificar sus factores asociados. Se realizó un estudio ecológico mixto con 166603 sujetos. La descripción se realizó con frecuencias, series de tiempo con las seroprevalencias y sus intervalos de confianza del 95 %. Se estimaron razones de odds crudas y ajustadas mediante regresión logística binaria en SPSS 25.0®. La seroprevalencia fue 0,567 % (IC 95 % = 0,53-0,60) con una endemia baja y estable desde el 2010. Los únicos factores que presentaron diferencias estadísticas en la seroprevalencia fueron el grupo etario y la frecuencia de donación, con una infección 23 % mayor en los donantes con edad mayor de 40 años (frente a las personas con edad entre 18-40), y 94 % mayor en los donantes de primera vez, en comparación con quienes donan a repetición . Se concluye que en Medellín los niveles endémicos del VHC han sido estables y bajos en la última década, evidenciando la importancia de la vigilancia epidemiológica que realizan los bancos de sangre. La menor prevalencia en la última década hace suponer una exposición diferencial al virus en función de la generación a la que se pertenece, de manera que el efecto de cohorte de nacimiento debe ser investigada en estudios posteriores.

ABSTRACT The objective of this study was to estimate the seroprevalence of hepatitis C virus (HCV) in donors of a Medellín-Colombia blood bank in the 2005-2018 period and to identify its associated factors. A mixed ecological study was conducted with 166603 donors. The description was made with frequencies, time series with seroprevalences and their 95 % confidence intervals. Odds ratios were estimated raw and adjusted by binary logistic regression in SPSS 25.0®. The seroprevalence was 0.567 % (95 % CI = 0.53-0.60) with a low and stable endemicity since 2010. The only factors that presented statistical differences in seroprevalence were the age group and the frequency of donation, with an infection 23 % higher in donors aged over 40 years (compared to people aged 18-40), and 94 % higher in first-time donors, compared to repeat ones. It is concluded that in Medellín the endemic levels of HCV have been stable and low in the last decade, evidencing the importance of the epidemiological surveillance carried out by blood banks. The lower prevalence in the last decade suggests a differential exposure to the virus depending on the generation to which it belongs, so that the birth cohort effect that should be studied in later research.

Meta-analyses of the validity and performance of screening tests for Hepatitis C Virus in the blood banks, 2000-2018 / Metaanálisis de la validez y el desempeño de las pruebas de tamización del virus de la hepatitis c en bancos de sangre, 2000-2018

RESUMEN Este estudio evaluó la validez y desempeño del inmunodiagnóstico del virus de la hepatitis C (VHC), con base en estudios publicados en la literatura científica mundial. Se diseñó y validó un protocolo de búsqueda y selección de investigaciones en las fases de la guía PRISMA, se analizaron los parámetros de sensibilidad, especificidad, cocientes de probabilidad, razón de odds y curva ROC, en MetaDisc. Se tamizaron 4602 estudios, de los cuales sólo 545 se realizaron en bancos de sangre y 18 evaluaron la validez diagnóstica de las pruebas para el VHC. La mayoría de los estudios fueron de Europa y Asia, con un 78 % basados en determinación de anticuerpos. Los estudios con detección de anticuerpos se realizaron en 21 483 donantes sanos y 3 145 infectados en quienes se halló una sensibilidad de 97,8 % (IC 95 % = 97,3 - 98,2), especificidad 99,0 % (IC 95 % = 98,9 - 99,2), cociente de probabilidad positivo 75,4 (IC 95 % = 27,2 - 209,2) y negativo de 0,02 (IC 95 % = 0,01 - 0,07) y área bajo la curva de 99,8 %. Se concluye que la detección de anticuerpos presenta excelente validez, desempeño y utilidad diagnóstica para la detección del VHC en donantes de sangre y población general.

ABSTRACT This study evaluated the validity and performance of the immunodiagnosis of the Hepatitis C Virus (HCV), based on studies published in the worldwide scientific literature. A search and selection research protocol was designed and validated in the phases of the PRISMA guide, the parameters of sensitivity, specificity, likelihood ratios, odds ratio, and ROC curve were analyzed in MetaDisc. 4602 studies were screened, of which only 545 were performed in blood banks and 18 evaluated the diagnostic validity of the tests for HCV. Most studies were from Europe and Asia, with 78 % based on antibody determination. Studies with antibody detection were carried out in 21483 healthy donors and 3145 infected patients in whom a sensitivity of 97.8 % (95 % CI = 97.3 - 98.2) was found, 99.0 % specificity (95 % CI = 98.9 - 99.2), positive likelihood ratio 75.4 (95 % CI = 27.2 - 209.2) and negative of 0.02 (95% CI = 0.01 - 0.07) and area under the curve 99.8 %. It is concluded that the detection of antibodies presents excellent validity, performance, and diagnostic utility for the detection of HCV in blood donors and the general population.

Rapid Antigen Detection Test for Diagnosis of Bacterial Pharyngitis / 대한내과학회지

Pharyngitis is a prevalent disease of the upper respiratory tract that requires treatment with an antibiotic. Group A streptococci (GAS) are the most frequent etiologic agents of bacterial pharyngitis. Because GAS are susceptible to penicillin, routine antibiotic susceptibility testing is not needed. Generally, patients with bacterial pharyngitis have high fever, cervical lymphadenopathy and tenderness, and tonsillar exudative discharge without symptoms of the common cold (e.g., cough, rhinorrhea, and sneezing). However, differentiating bacterial pharyngitis from viral pharyngitis based only on their clinical manifestations is problematic. Therefore, a bacterial culture or a rapid antigen detection test (RADT) is required for the diagnosis of bacterial pharyngitis. Although bacterial culture is the gold standard for diagnosis of bacterial pharyngitis, its accuracy is affected by the technical expertise of the technician, and there is a delay of 1–2 days before the results become available. In contrast, the sensitivity of RADT has increased to over 90%, making them suitable for screening purposes. The result of a RADT is available within 5–10 minutes, obviating the need for a second visit to obtain the results of culture. Use of a RADT would enable the optimal antibiotic to be administered earlier, reducing the overuse of antibiotics.

Interferon-gamma release assay versus tuberculin skin test for latent tuberculosis infection among HIV patients in Brazil

Abstract Setting Patients HIV+ attending in a reference clinic, Southern Brazil. Objective To compare the interferon-gamma-release assay (IGRA – QuantiFERON® TB Gold In-Tube) with the tuberculin skin test (TST – PPD-Rt 23) for latent tuberculosis infection (LTBI) in patients with HIV. Design Cohort study. Patients were simultaneously submitted to the TST and blood collection for the IGRA. Results A total of 140 subjects were included. Nine (6.4%) were IGRA+/TST+, 12 (8.6%) were IGRA+/TST−, 4 (3%) were IGRA−/TST+, and 115 (82%) IGRA−/TST−. There was poor agreement between tests (kappa = 0.2), and no correlation between these results and CD4+ T lymphocyte counts. During follow-up, one patient with negative results on both tests died from sepsis, and another with discordant results (IGRA+/TST−) exhibited TST seroconversion. Compared to the TST, IGRA showed a sensitivity and specificity of 69% and 90%, respectively. The IGRA detected 8% more positive results than the TST. All patients were followed up for 2 years. Conclusion The higher accuracy of the IGRA would result in LTBI treatments being administered to patients who would have otherwise been overlooked, decreasing the number of active tuberculosis cases. The long-term survival of HIV carriers requires further evaluation.

Summary of the 2011 national autoantibody testing quality control / 中华风湿病学杂志

Objective To consecutively investigate the quality of auto-antibody testing of the whole country and to improve quality.Methods A nation-wide investigation was carried out and hospitals or departments participating were notified by letter or telephone communication.Autoantibodies tested for quality control survey included anti-nuclear antibody (anti-ANA),anti-double-stranded DNA (anti-dsDNA)antibody,anti-extractable nuclear antigens (anti-ENA) antibody,anti-mitochondria antibody (AMA),anti-smooth muscle antibody (ASMA) and anti-citrulline antibody (anti-CCP).There were 15 samples in total for testing,including 3 control samples for each test.Same sample was used for both AMA and ASMA test.Sample distribution and data analysis were carried out double-blindly.A total of 114 hospitals or departments participated in the survey.Multiple testing methods were adopted including indirect immumo-fluo-rescence (IIF),immuno-blot (IB),dot-blot (DB),double immuno-diffusion (DID),enzyme linked immuno-sorbent assay (ELISA),chemiluminescent assay,dot-immunogold filtration assay.Results The accurate rates for this survey were 98％,96.6％,89.5％,98.1％,92.1％,96.4％ respectively for ANA,anti-dsDNA,anti-ENA,AMA,ASMA and anti-CCP.Anti-ENAs were further divided into anti-RNP,anti-Sm,anti-SSA,anti-SSB and anti-Scl-70 subgroups,and the accurate rates were 88.4％,96.8％,100％,100％ and 95.8％,respectively.Titers of ANA varied greatly among different labs,so did quantitative analysis of anti-CCP,AMA and antidsDNA by ELISA.However,the accuracy of ANA types determined by IIF was greatly improved.Detection rate of AMA and AMSAwas still low.Conclusion Among detected antibodies,ANA,anti-dsDNA and antiCCP are the most prominently improved.Accurate rate of anti-ENA antibody is slightly increased.

Retrospective seroepidemiological analysis of patients with suspicion of paracoccidioidomycosis in São Paulo State, Brazil

The geographic distribution of paracoccidioidomycosis (PCM) in the Brazilian state of São Paulo was evaluated in a retrospective study using secondary data from serological analyses, carried out by double immunodiffusion assay of patients with PCM suspicion, from January 1999 to May 2010. Sixty percent of 10,176 patients, from 239 cities, were serologically reactive to P. brasiliensis. The cities that showed the most serological reactivity among patients were São João da Boa Vista (85%), Piracicaba (75%), Sorocaba (73%), Campinas (72%) and São Paulo (62%). São Paulo state has an area of 248,209.4 km²; the climate is tropical and sub-tropical with annual temperatures between 18 and 24ºC, high rainfall (900 to 1800 mm/year), rainy summers and mild winters. It also features large areas composed of acidic soils, and is one of the greatest contributors to Brazilian agricultural production and, separately, the largest producer of orange juice and, the ninth greatest producer of soy and sugar cane and the fourth largest coffee producer. We suggest that the climatic characteristics associated with soil type and development of primary activities can contribute to the endemic potential of PCM in São Paulo state.

Histoplasmosis localizada del sistema nervioso central en un niño inmunocompetente / Central nervous system localized histoplasmosis in an immunocompetent child

Introducción. La histoplasmosis localizada del sistema nervioso en una forma rara de presentación de estamicosis sistémica. Se puede manifestar clínicamente como una meningitis crónica, lesiones focales encefálicas ode la médula espinal, ataques cerebrovasculares y encefalitis. Caso clínico. Se presenta el caso de un niño inmunocompentente con histoplasmosis localizada del sistema nervioso central. Su cuadro clínico neurológico fue de evolución crónica y presentó varios déficits neurológicos focales. Las imágenes diagnósticas evidenciaron múltiples masas del tallo cerebral y de la médula espinal cervical. Las pruebas inmunológicas demostraron anticuerpos anti Histoplasma. El paciente mejoró con el tratamiento secuencial de anfotericina B y fluconazol. Conclusiones. A pesar de su rareza, la histoplasmosis del sistema nervioso debe estar en el diagnóstico diferencial de las masas múltiples del encéfalo y médula espinal en un paciente residente en área endémica, las pruebas inmunológicas son útiles como herramienta diagnóstica y el tratamiento antimicótico puede llevar a la curación.

Introduction. Localized central nervous system histoplasmosis is a rare clinical form of this systemic mycosis. It could be presented as chronic meningitis, focal encephalic or spinal cord lesions, stroke syndromes and encephalitis.Clinical case. We present a case of an immunocompetent child with localized histoplasmosis of the central nervous system. The neurological case had a chronic evolution and presented several focal neurological deficits. Magnetic resonance imaging showed multiple masses of the brainstem and the cervical spinal cord. Immunologicaltests showed antibodies anti-Histoplasma capsulatum. The clinical condition of the patient improved with the sequential treatment with amphotericin B and fluconazole.Conclusions. In spite of the rare presentation, central nervous system histoplasmosis should be considered inthe differential diagnosis of multiple brain and spinal cord lesions in a patient resident in an endemic area. Immunological tests are useful as a diagnostic tool and the antifungal treatment could lead to cure.

Un problema de diagnóstico perinatal: pacientes serológicamente negativos pero infectados por el VIH / A perinatal diagnostic problem: HIV infected patients who are serologically negative

A 142 pacientes se les realizó ELISA, Inmuno blot de IgG, Inmuno blot de IgA (en los menores de 24 meses), determinación de antígeno en plasma, aislamiento viral por cultivo de detección de genoma viral por amplificación con la reacción de polimerasa en cadena (PCR). El diagnóstico integral demostró que 10 por ciento (14 pacientes) que resultaron negativos o indeterminados para detección de anticuerpos IgG anti-VIH-1, estaban infectados por el virus. Once de estos pacientes tienen entre 2 y 24 meses de edad; dos, entre 4 y 6.5 años, y uno, 30 años. El diagnóstico se emitió en cuatro de los casos por presencia de antígeno en plasma; en cinco por amplificación por PCR de ADN proviral presente en células mononucleares periféricas; en cuatro casos por PCR positivo e inmunofluorescencia (IF) del cultivo, y el último caso, presentó Inmuno blot positivo e IF del cultivo. Dichos casos presentan el problema de resultados falsos negativos por serología de anticuerpos anti-VIH, especialmente en niños menores de 24 meses

Comprehensive HIV diagnosis of 142 patients was done by ELISA, IgG immunoblot, IgA immunoblot (in patients under 24 months), plasma antigen determination, viral isolation by culture and genome detection by polymerasa chain reaction (PCR) amplification. Results showed that 14 patients (10%) with negative or indefinite results for anti-HIV-1 IgG antibody were in fact infected by the virus. Eleven of these patients were between 2 and 24 months of age, two between 4 and 6.5 years and one was 30 years old. Diagnosis was obtained by antigen positivity in four of them; by PCR amplification of peripheral mononuclear cells of proviral DNA in five of them; by PCR and immunofluorescence (II) of cultured cells in four cases, and the last diagnosis was made by IgG immunoblot and IF of the viral culture. These cases pose a problem because of false negative HIV serology, particularly in patients under 24 months of age.

Clinical significance of the immunological tests in rheumatoid arthritis

Of the many theoretical causes of rheumatoid arthritis(RA), the most widely held theory is the autoimmune mechanism. In order to clarify the clinical significance of the immunological tests in RA, we studied immunoglobulin and complement levels in sera and synovial fluids of 118 RA patients and the following results were obtained. 1) The levels of immunoglobulins were elevated in both serum and synovial fluid and this was more prominent in the seropositive cases than the seronegative ones. 2) The levels of C3 component were decreased in both serum and synovial fluid, while those of C4 were decreased only in synovial fluid. Serum C3 and C4 component levels were more decreased in the seropositive cases than the seronegative ones. 3) The immunoglobulin levels in serum (IgG, IgM and IgA) and synovial fluid (IgG and IgA) and the levels of C3, C4 component in serum were well correlated with the clinical forms of rheumatoid arthritis. 4) The IgA level in serum and IgM level in synovial fluid were more increased in the exacerbated cases than the chronic ones. 5) Serum IgG level was decreased after steroid medication over one month.