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1.
Article in Chinese | WPRIM | ID: wpr-936146

ABSTRACT

OBJECTIVE@#To evaluate the effects of hepatitis B virus (HBV) on helper T lymphocytes 17 (Th17), regulatory T lymphocyte (Treg) and Th17/Treg ratio in chronic hepatitis B patients in different alanine aminetransferase (ALT) stages.@*METHODS@#In the study, 336 chronic hepatitis B patients in the first hospital of Lanzhou University were analyzed. The hepatitis B antigen antibody parameters were measured by chemiluminescence immunoassay analyzer, the liver function parameters were measured by automatic biochemical analyzer, the HBV loads were measured by quantitative PCR, Th17, Treg and Th17/Treg ratios were detected by flow cytometry. Among them, 111 cases (ALT < 40 U/L) of ALT were normal hepatitis B, 108 cases of chronic hepatitis B with ALT above normal upper limit and < 2 times higher (40 U/L≤ALT < 80 U/L), and 117 cases of chronic hepatitis B with ALT above 2 times normal upper limit (80 U/L≤ALT). According to the viral load, they were divided into low replication group with HBV DNA < 4.0 lg copies/mL, medium replication group with 4.0 lg copies/mL≤HBV DNA < 6.0 lg copies/mL and high replication group with HBV DNA ≥ 6.0 lg copies / mL. Dunnett T3 variance analysis were used to analyze the effects of HBV on Th17, Treg and Th17/Treg ratio in the chronic hepatitis B patients in different ALT stages. The changes of virological and immunological indexes before and after treatment were observed for 24 weeks of antiviral therapy in the hepatitis B patients with ALT≥double upper limit of normal group.@*RESULTS@#In the ALT normal group, different virus load HBV had minor effects on Th17, Treg and Th17/Treg ratio. In the ALT≥2 times upper limit of normal group, with the virus load increased, Th17 (3.18%±0.79% in low replication group, 3.78%±0.92% in medium replication group and 4.57%±1.15% in high replication group), Treg cells (5.52%±1.58% in low replication group, 5.89%±1.84% in medium replication group and 6.37%±2.35% in high replication group) and their ratio Th17/Treg (0.57±0.25 in low replication group, 0.65±0.29 in medium replication group and 0.73±0.36 in high replication group) were significantly increased (P < 0.05). After entecavir treatment 24 weeks, the patient' s HBV-DNA decreased significantly, Th17 (3.89%±1.02% vs. 2.06%±0.46%), Treg (6.02%±2.03% vs. 5.06%±1.25%), Th17/Treg ratio (0.65±0.28 vs. 0.41±0.14) decreased significantly (P < 0.05).@*CONCLUSION@#Investigation on the effects of HBV on Th17 and Treg cells and their ratios in different ALT states can clarify the effects of HBV on the body from the immunological perspective and can further understand the ALT grouping for antiviral treatment theoretical significance, which is helpful for clinical treatment.


Subject(s)
Humans , Alanine/therapeutic use , Alanine Transaminase/therapeutic use , Antiviral Agents/therapeutic use , DNA, Viral/therapeutic use , Hepatitis B/drug therapy , Hepatitis B virus/genetics , Hepatitis B, Chronic/drug therapy , T-Lymphocytes, Regulatory
2.
Chinese Journal of Hepatology ; (12): 99-102, 2022.
Article in Chinese | WPRIM | ID: wpr-935916

ABSTRACT

Covalently closed circular DNA (cccDNA) of hepatitis B virus (HBV) is the template for HBV replication. Currently, there is a lack of therapeutic drugs that directly target cccDNA. Therefore, blocking cccDNA supplements as fast as possible and reducing the existing cccDNA is the key to achieving a complete cure of chronic hepatitis B. Previous studies have suggested that cccDNA had a long half-life, but a recent study showed that it only took a few months to update cycle of cccDNA pool, and its number was much less than previously predicted. In the future, with the advent of new antiviral drugs that can completely inhibit HBV replication, it is expected that the cccDNA pool will be completely cleared due to its supplement complete blockade, so as to achieve virological cure of chronic hepatitis B.


Subject(s)
Humans , Antiviral Agents/therapeutic use , DNA, Circular/genetics , DNA, Viral , Half-Life , Hepatitis B/drug therapy , Hepatitis B virus/genetics , Hepatitis B, Chronic/drug therapy , Virus Replication
4.
Chinese Journal of Hepatology ; (12): 429-438, 2022.
Article in Chinese | WPRIM | ID: wpr-928467

ABSTRACT

Hepatitis B virus (HBV) infection remains to be the major cause of chronic liver diseases in China. Since the nucleos(t)ide analogues and pegylated interferon-alpha do not directly target the covalently closed circular DNA (cccDNA) in the nuclei of HBV-infected hepatocytes, those standard-of-care medications cannot efficiently cure the infected hepatocytes and rarely achieve the functional cure of chronic hepatitis B (CHB). Therefore, new antiviral drugs targeting distinct steps of HBV replication and immunotherapeutics reinvigorating antiviral immune responses are urgently needed for the functional cure of CHB. Based on the extensive discussion of the biological and clinical significance of new virologic biomarkers and distinct mechanism of drug candidates currently in clinical development, we propose that the selection of virologic and immunological biomarkers for evaluation of therapeutic efficacy as well as setting the therapeutic endpoints in the clinical trials should be based on the mode of action of investigational drugs. In addition, due to the complexity of CHB pathogenesis, selection of specific subpopulation of CHB patients for the clinical trials of drugs with a specific mode of action should also be considered.


Subject(s)
Humans , Antiviral Agents/therapeutic use , Biomarkers , DNA, Circular , DNA, Viral , Hepatitis B/drug therapy , Hepatitis B Surface Antigens , Hepatitis B virus/genetics , Hepatitis B, Chronic , Virus Replication
5.
Chinese Journal of Biotechnology ; (12): 1039-1049, 2022.
Article in Chinese | WPRIM | ID: wpr-927761

ABSTRACT

Hepatitis B virus core protein (HBc) has become a hot spot in drug carrier protein research due to its natural particle self-assembly ability and ease of modification. The truncation of the C-terminal polyarginine domain (CTD, aa 151-183) of HBc does not affect the self-assembly of the particles. However, it does affect the internal and external charges of the particles, which may subsequently affect drug encapsulation. Thus, the truncated C-terminal polyarginine domain (CTD) of HBc and the inserted RGD peptide were selected to construct and express three HBc variants (RH) encapsulated with ICG (RH/ICG) with different C-terminal lengths to compare the stability and drug activity of their nanoformulations. RH160/ICG was found to have a great advantages in encapsulation efficiency and biological imaging. Compared with other HBc variants, RH160/ICG significantly improved encapsulation efficiency, up to 32.77%±1.23%. Cytotoxicity and hemolysis assays further demonstrated the good biocompatibility of RH160/ICG. Cell uptake and in vivo imaging experiments in mice showed that RH160/ICG could efficiently deliver ICG in tumor cells and tumor sites with good imaging effect. This research provides a new direction for further expanding the diagnosis and treatment application of ICG and development of HBc-based nanoparticle drug carrier platform.


Subject(s)
Animals , Mice , Hepatitis B/drug therapy , Hepatitis B Core Antigens , Indocyanine Green/chemistry , Nanoparticles/chemistry , Viral Core Proteins
6.
Chinese Medical Journal ; (24): 571-583, 2022.
Article in English | WPRIM | ID: wpr-927536

ABSTRACT

Chronic hepatitis B virus (HBV) infection remains a global health burden. Timely and effective antiviral therapy is beneficial for patients with HBV infection. With existing antiviral drugs, including nucleos(t)ide analogs and interferon-alfa, patients can achieve viral suppression with improved prognosis. However, the rate of hepatitis B surface antigen loss is low. To achieve a functional cure and even complete cure in chronic hepatitis B patients, new antivirals need to be developed. In this review, we summarized the advantages and disadvantages of existing antiviral drugs and focused on new antivirals including direct-acting antiviral drugs and immunotherapeutic approaches.


Subject(s)
Humans , Antiviral Agents/therapeutic use , Hepatitis B/drug therapy , Hepatitis B Surface Antigens , Hepatitis B virus , Hepatitis B, Chronic/drug therapy , Hepatitis C, Chronic/drug therapy
7.
Washington; OPS; jul. 2020. 64 p.
Non-conventional in Spanish | BIGG, LILACS | ID: biblio-1393166

ABSTRACT

Según estimaciones de la Organización Mundial de la Salud (OMS), en el 2015 257 millones de personas en el mundo tenían la infección crónica por el virus de la hepatitis B (VHB) y 900 000 fallecieron a causa de ella, en la mayor parte de los casos de cirrosis o carcinoma hepatocelular. La mayoría de las defunciones asociadas con el VHB en personas adultas obedecen a infecciones contraídas al nacer o en los cinco primeros años de vida. En mayo del 2016, la Asamblea Mundial de la Salud aprobó la Estrategia mundial del sector de la salud contra las hepatitis víricas 2016-2021, en la que se hace un llamado a eliminar las hepatitis virales como amenaza de salud pública ­definida como una reducción de 90% de la incidencia de infecciones y una reducción de 65% de la mortalidad­ para el 2030. La eliminación de la infección por el VHB como amenaza de salud pública conlleva la necesidad de reducir la prevalencia del antígeno de superficie del virus de la hepatitis B (HBsAg) a menos de 0,1% en los niños de 5 años de edad. Esta meta se puede lograr mediante la vacunación de todos los recién nacidos contra la hepatitis B y otras intervenciones orientadas a prevenir la transmisión maternoinfantil del VHB


Subject(s)
Humans , Female , Pregnancy , Infectious Disease Transmission, Vertical/prevention & control , Hepatitis B/drug therapy , Antiviral Agents/therapeutic use , Pregnancy/drug effects , Tenofovir/pharmacology , Hepatitis B e Antigens/analysis
8.
Frontiers of Medicine ; (4): 495-505, 2021.
Article in English | WPRIM | ID: wpr-888737

ABSTRACT

On the basis of real-world clinical data, the study aimed to explore the effect and mechanisms of the treatment plan of "traditional Chinese medicine (TCM) regulating liver regeneration." A total of 457 patients with HBV-related liver failure were retrospectively collected. The patients were divided into three groups: the modern medicine control group (MMC group), patients treated with routine medical treatment; the control group combining traditional Chinese and Western medicine (CTW), patients treated with routine medical treatment plus the common TCM formula; and the treatment group of "TCM regulating liver regeneration" (RLR), patients treated with both routine medical treatment and the special TCM formula of RLR. After 8 weeks of treatment, the mortality of patients in the RLR group (12.31%) was significantly lower than those in the MMC (50%) and CTW (29.11%) groups. Total bilirubin level significantly decreased and albumin increased in the RLR group when compared with the MMC and CTW groups (P < 0.05). In addition, there were significant differences in the expression of several cytokines related to liver regeneration in the RLR group compared with the MMC group. RLR treatment can decrease jaundice, improve liver function, and significantly reduce the mortality in patients with HBV-related liver failure. The mechanism may be related to the role of RLR treatment in influencing cytokines related to liver regeneration.


Subject(s)
Humans , Drugs, Chinese Herbal/therapeutic use , Hepatitis B/drug therapy , Liver Failure , Liver Regeneration , Medicine, Chinese Traditional , Retrospective Studies
9.
Braz. j. infect. dis ; 24(5): 434-451, Sept.-Oct. 2020. tab
Article in English | LILACS, ColecionaSUS | ID: biblio-1142552

ABSTRACT

Abstract Chronic hepatitis B is an important health problem that can progress to cirrhosis and complications such as hepatocellular carcinoma. There is approximately 290 million of people with chronic hepatitis B virus (HBV) infection worldwide, however only 10% of patients are currently identified.Most part of Brazil is considered of low prevalence of HBV infection but there are some regions with higher frequency of carriers. Unfortunately, many infected patients are not yet identified nor evaluated for treatment.The Brazilian Society of Infectious Diseases (SBI) and the Brazilian Society of Hepatology worked together to elaborate a guideline for diagnosis and treatment of hepatitis B. The document includes information regarding the population to be tested, diagnostic tools, indications of treatment, therapeutic schemes and also how to handle HBV infection in specific situations (pregnancy, children, immunosuppression, etc).Delta infection is also part of the guideline, since it is an important infection in some parts of the country.


Subject(s)
Child , Female , Humans , Pregnancy , Hepatitis B, Chronic , Gastroenterology , Hepatitis B , Liver Neoplasms , Brazil , Hepatitis B virus , Hepatitis B, Chronic/diagnosis , Hepatitis B, Chronic/drug therapy , Hepatitis B/diagnosis , Hepatitis B/drug therapy
10.
Rev. Soc. Bras. Med. Trop ; 49(1): 24-28, Jan.-Feb. 2016. tab
Article in English | LILACS | ID: lil-776535

ABSTRACT

Abstract: INTRODUCTION: Few studies have addressed the primary characteristics of patients infected with hepatitis B virus (HBV) in the general population, especially those living in small- and medium-sized cities in Brazil. We aimed to determine the clinical, demographic, and epidemiologic characteristics of patients diagnosed with HBV who were followed up at an infectious diseases clinic of a public hospital in State of São Paulo, Brazil. METHODS: Medical records of patients aged >18 years and diagnosed with HBV infection between January 2000 and December 2013 were reviewed. RESULTS: Seventy-five patients were enrolled with male-female main infection-associated risk factors; 9 (12%) were co-infected with human immunodeficiency virus (HIV), 5 (6.7%) with hepatitis C virus (HCV), and 3 (4%) were co-infected with both HIV and HCV. Antiviral HBV therapy was applied in 21 (28%) patients and tenofovir monotherapy was the most prescribed medication. After approximately 2 years of antiviral treatment, the HBV-DNA viral load was undetectable in 12 (92.3%) patients and lower levels of alanine aminotransferase were found in these patients. CONCLUSIONS: Over a 13-year interval, very few individuals infected with HBV were identified, highlighting the barriers for caring for patients with HBV in developing countries. New measures need to be implemented to complement curative practices.


Subject(s)
Humans , Male , Female , Adult , Hepatitis B/epidemiology , Socioeconomic Factors , Brazil/epidemiology , Acute Disease , Chronic Disease , Retrospective Studies , Risk Factors , Cohort Studies , Viral Load , Alanine Transaminase , Hepatitis B/diagnosis , Hepatitis B/drug therapy , Hospitals, Public , Middle Aged
11.
Sâo Paulo med. j ; 133(6): 525-530, Nov.-Dec. 2015. tab, graf
Article in English | LILACS | ID: lil-770149

ABSTRACT

CONTEXT: Orthotopic liver transplantation (OLT) is the treatment of choice for end-stage liver disease. Cirrhosis due to hepatitis C infection is the leading indication for liver transplantation worldwide. However, patients who are given transplants because of viral liver diseases often present clinical coinfections, including hepatitis B together with hepatitis D. Currently, different strategies exist for patient management before and after liver transplantation, and these are based on different protocols developed by the specialized transplantation centers. CASE REPORT: We present a rare case of a 58-year-old man with chronic hepatitis B, C and D coinfection. The patient developed cirrhosis and hepatocellular carcinoma. His treatment comprised antiviral therapy for the three viruses and OLT. The patient's outcome was satisfactory. CONCLUSION: OLT, in association with antiviral therapy using entecavir, which was administered before and after transplantation, was effective for sustained clearance of the hepatitis B and D viruses. A recurrence of hepatitis C infection after transplantation responded successfully to standard treatment comprising peginterferon alfa-2A and ribavirin.


CONTEXTO: O transplante ortotópico de fígado (TOF) é o tratamento de escolha em pacientes com doença hepática terminal. A cirrose por hepatite C é a principal indicação de transplante hepático no mundo. No entanto, pacientes transplantados por hepatopatias virais frequentemente apresentam coinfecções, como hepatite B associada a hepatite D. Atualmente, existem diferentes estratégias de manejo em pacientes pré e pós-transplantados conforme diferentes protocolos de conduta de serviços especializados em transplante. RELATO DE CASO: Apresentamos o raro caso de um homem de 58 anos diagnosticado com as hepatites crônicas B, C e D. O paciente evoluiu com cirrose e carcinoma hepatocelular. O tratamento consistiu de terapia antiviral para os três vírus e de transplante ortotópico de fígado. O desfecho do paciente foi satisfatório. CONCLUSÃO: O transplante ortotópico de fígado, associado à terapia antiviral com entecavir antes e após o procedimento, foi eficaz na depuração sustentada dos vírus B e D. A recidiva do vírus C após o transplante respondeu com sucesso ao tratamento padrão com alfapeginterferon 2A e ribavirina.


Subject(s)
Humans , Male , Middle Aged , Carcinoma, Hepatocellular/surgery , Hepatitis, Viral, Human/drug therapy , Hepatitis, Viral, Human/surgery , Liver Cirrhosis/surgery , Liver Neoplasms/surgery , Liver Transplantation/methods , Antiviral Agents/therapeutic use , Coinfection/drug therapy , Coinfection/surgery , Hepatitis B/drug therapy , Hepatitis B/surgery , Hepatitis C/drug therapy , Hepatitis C/surgery , Hepatitis D/drug therapy , Hepatitis D/surgery , Interferon-alpha/therapeutic use , Liver Cirrhosis/virology , Polyethylene Glycols/therapeutic use , Recurrence , Recombinant Proteins/therapeutic use , Ribavirin/therapeutic use , Treatment Outcome
12.
Article in English | WPRIM | ID: wpr-223872

ABSTRACT

Recurrence of viral hepatitis after liver transplantation (LT) can progress to graft failure and lead to a decrease in long-term survival. Recently, there have been remarkable improvement in the treatment of chronic hepatitis B (CHB) using potent antiviral agents. Combination of hepatitis B immunoglobulin and potent antiviral therapy has brought marked advances in the management of CHB for liver transplant recipients. Post-transplant antiviral therapy for hepatitis C virus infection is generally reserved for patients showing progressive disease. Acheiving a sustained virological response in patients with LT greatly ameliorates graft and overall survival, however this only occurs in 30% of transplant recipient using pegylated interferon and ribavirin (RBV). Direct acting antivirals such as protease inhibitors, polymerase or other non-structural proteins inhibitors are anticipated to establish the new standard of care for transplant recipients. In liver transplant recipients, hepatitis E virus infection is an uncommon disease. However, it can lead to chronic hepatitis and cirrhosis and may require retransplantation. Recently, 3-month course of RBV monotherapy has been reported as an effective treatment. This review focuses on the recent management and therapeutic approaches of viral hepatitis in liver transplant recipient.


Subject(s)
Humans , Antiviral Agents/therapeutic use , Hepatitis B/drug therapy , Hepatitis C/drug therapy , Hepatitis E/drug therapy , Hepatitis, Viral, Human/drug therapy , Liver Transplantation , Recurrence
13.
Article in English | WPRIM | ID: wpr-106801

ABSTRACT

BACKGROUND/AIMS: Occult HBV infection can persist following HBsAg loss and be transmitted, but the virological features are not well defined. METHODS: Here we investigated 25 Korean patients who lost HBsAg during follow up, either spontaneously or subsequent to therapy. RESULTS: Whereas subtype adr (genotype C) was found in 96% of HBsAg positive patients, 75 % of patients who lost HBsAg spontaneously were seemed to be infected with the ayw subtype with sequence similar to genotype D. Mutations in the major hydrophilic region (MHR) of HBsAg were found in 7 patients who lost HBsAg spontaneously. The mutations include T123S, M125I/N, C139R, D144E, V177A, L192F, and W196L, some of which have not been reported before. Functional analysis via transfection experiments indicate that the C139R and D144E mutations drastically reduced HBsAg antigenicity, while the Y225del mutation found in one interferon-treated patient impaired HBsAg secretion. CONCLUSIONS: Lack of detectable HBsAg in patient serum could be explained by low level of ccc DNA in liver tissue, low antigenicity of the surface protein, or its secretion defect.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Amino Acid Sequence , Antiviral Agents/therapeutic use , DNA, Circular/analysis , Genotype , Hep G2 Cells , Hepatitis B/drug therapy , Hepatitis B Surface Antigens/blood , Hepatitis B virus/genetics , Liver/virology , Molecular Sequence Data , Mutation , Remission, Spontaneous , Republic of Korea , Serotyping
14.
Rev. Soc. Bras. Clín. Méd ; 10(3)maio-jun. 2012.
Article in Portuguese | LILACS | ID: lil-621489

ABSTRACT

JUSTIFICATIVA E OBJETIVOS: As hepatites causadas pelos vírus da hepatite B (VHB), vírus da hepatite C (VHC) e vírus da hepatite (VHD) têm como aspecto comum a transmissão por via parenteral e a possibilidade de cronificação. Revisar os aspectos clínico-epidemiológicos, diagnósticos, terapêuticos e profiláticos das infecções virais por tais agentes é o escopo do presente artigo. Realizou-se pesquisa bibliográfica nas bases de dados Scielo e Pubmed empregando-se os descritores hepatite B (hepatitis B); hepatite C (hepatitis C); hepatite D (hepatitis D) e hepatite G (hepatitis G), assim como livros texto, consensos e diretrizes relacionadas ao tema.CONTEÚDO: As formas agudas das hepatites B, C e D são usualmente benignas, podendo, sem embargo, ocorrerem quadros de hepatite fulminante. Em situações nas quais o sistema imunológico não é capaz de depurar o VHB e/ou VHC, há cronificação da infecção, com risco de desenvolvimento de cirrose e consequente insuficiência hepática crônica, bem como carcinoma hepatocelular. As hepatites B e D são imunopreveníveis, graças à vacina parao vírus B, mas, até o momento, não há imunoprofilaxia disponível para o vírus C.CONCLUSÃO: As hepatites pelos VHB e VHC constituem importantes desafios para a medicina atual, especialmente pela prevalência das infecções no planeta e pelo risco de desenvolvimento das complicações crônicas. Neste contexto, destaque-se a importância da avaliação diagnóstica, da instituição da terapêutica adequada e do emprego das medidas preventivas para tais infecções, elementos que devem ser solidamente conhecidas pelo clínico.


BACKGROUND AND OBJECTIVES: Hepatitis caused by hepatitis B virus (HBV), hepatitis C virus (HCV) and hepatitis D virus (HDV) have in common the transmission by parenteral route and the possibility of chronification. Reviewing the clinic, epidemiology, diagnose, therapeutics and prophylaxis of viral infections by these agents is the scope of this work. Bibliographic research was conducted both at databases Scielo and Pubmed through the chosen descriptors: hepatitis B, hepatitis C, hepatitis D and hepatitis G, and text books, consensus and guidelines related to the subject.CONTENTS: The acute viral B, C and D hepatitis are usually benign, though acute liver failure, fulminant hepatitis, may occur. In the cases when the immune system is unable to debug HBV and HCV the infection becomes chronic, cirrhosis with consequent chronic liver insufficiency and hepatocellular carcinomamay develop. HBV and HDV are immunopreventable, thanks to the hepatitis B virus vaccine, but at this point there's no immunoprophylaxis available for hepatitis C virus. CONCLUSION: HBV and HCV hepatitis are great challenges for medicine, particularly due to the prevalence of infections worldwide and the risk of chronic complications. In this context, diagnostic evaluation, adequate therapeutic care, and preventive measures must be soundly known by the physician.


Subject(s)
Humans , Hepatitis B/epidemiology , Hepatitis B/etiology , Hepatitis B/drug therapy , Hepatitis C/epidemiology , Hepatitis C/etiology , Hepatitis C/drug therapy , Hepatitis D/epidemiology , Hepatitis D/etiology , Hepatitis D/drug therapy
15.
GEN ; 66(2): 114-117, jun. 2012. ilus, tab
Article in Spanish | LILACS | ID: lil-664212

ABSTRACT

Determinar la respuesta inmunológica a la vacunación contra virus de hepatitis B en pacientes pediátricos con enfermedad celíaca. Se revisaron 25 historias clínicas de celíacos diagnosticados entre 2001-2010 por estudios serológico, histopatológicos, genético y esquema de vacunación hepatitis B completo, de los cuales se excluyeron 11 pacientes. Se solicitó anticuerpo contra antígeno de superficie virus hepatitis B. El grupo de celíacos no respondedores fue evaluado posterior a revacunación bajo apego a dieta sin gluten. Se estudiaron 14 pacientes (35,7% hembras, 64,3% varones). 8 pacientes se vacunaron al nacer y 6 después de los 8 años de edad. De los cuales 28,6% tuvieron baja respuesta a la vacunación y 71,4% sin respuesta. La respuesta fue positiva en 3/8 (37,5%) de los pacientes vacunados al nacer y en 1/6 de los mayores de 8 años (16,7%). 4 no respondedores fueron revacunados cumpliendo dieta libre de gluten, evidenciándose respuesta inmunológica positiva en el 75%. Existe una disminución en la respuesta a la vacunación contra hepatitis B en pacientes celíacos, asociado a HLA DQ2 y que la dieta libre de gluten puede mejorar la respuesta inmunológica


To determine the immune response to the vaccination against hepatitis B virus in pediatric patients with celiac disease. Reviewed 25 medical histories of celiac diagnosed between 2001-2010 by serological, histopathological, genetic studies and full hepatitis B vaccination scheme, of which 11 patients were excluded. Also ask antibody against hepatitis B virus surface antigen The group of non-responder celiac was evaluated after revaccination under attachment to diet without gluten. 14 Patients were studied (35.7% females, 64.3% boys). 8 patients vaccinated at birth and 6 after eight years of age. Of which 28.6% had low response to vaccination and 71.4% unanswered. The answer was positive in 3/8 (37.5%) of patients vaccinated at birth and 1/6 of the 8 older (16.7%). not answering. 4 were fulfilling gluten-free diet, showing response immunological positive in 75%. There is a decrease in the response to vaccination against hepatitis B in celiac patients, conditional primarily by HLA DQ2 and that the gluten-free diet can improve the immune response


Subject(s)
Female , Child , Celiac Disease/diagnosis , Celiac Disease/immunology , Celiac Disease/drug therapy , Hepatitis B/immunology , Hepatitis B/drug therapy , Vaccination , Gastroenterology , Pediatrics , Malabsorption Syndromes/complications , Malabsorption Syndromes/diagnosis
16.
Article in English | WPRIM | ID: wpr-101282

ABSTRACT

Chronic liver disease represents a major public health problem, accounting for significant morbidity and mortality worldwide. As prognosis and management depend mainly on the amount and progression of liver fibrosis, accurate quantification of liver fibrosis is essential for therapeutic decision-making and follow-up of chronic liver diseases. Even though liver biopsy is the gold standard for evaluation of liver fibrosis, non-invasive methods that could substitute for invasive procedures have been investigated during past decades. Transient elastography (TE, FibroScan(R)) is a novel non-invasive method for assessment of liver fibrosis with chronic liver disease. TE can be performed in the outpatient clinic with immediate results and excellent reproducibility. Its diagnostic accuracy for assessment of liver fibrosis has been demonstrated in patients with chronic viral hepatitis; as a result, unnecessary liver biopsy could be avoided in some patients. Moreover, due to its excellent patient acceptance, TE could be used for monitoring disease progression or predicting development of liver-related complications. This review aims at discussing the usefulness of TE in clinical practice.


Subject(s)
Humans , Antiviral Agents/therapeutic use , Carcinoma, Hepatocellular/epidemiology , Chronic Disease , Elasticity Imaging Techniques , Hepatitis B/drug therapy , Hepatitis C/drug therapy , Liver Cirrhosis/diagnosis , Liver Neoplasms/epidemiology , Recurrence
17.
Article in English | WPRIM | ID: wpr-101274

ABSTRACT

Hepatitis B virus (HBV) may be reactivated after chemotherapy or immunosuppressive therapy, and therefore administration of antiviral agents before such treatment is recommended. Most reported cases of reactivation are associated with high doses of immunosuppressive agents or combination therapy. We present a case of a previously inactive HBV carrier with an acute severe flare-up during a long-term, very-low-dose (2.5 mg/day) steroid treatment for rheumatoid arthritis. We suggest that even a minimal dose of single-regimen oral steroid can cause reactivation of indolent, inactive HBV.


Subject(s)
Aged, 80 and over , Female , Humans , Antiviral Agents/therapeutic use , Arthritis, Rheumatoid/drug therapy , DNA, Viral/analysis , Hepatitis B/drug therapy , Hepatitis B Surface Antigens/blood , Hepatitis B virus/genetics , Immunosuppressive Agents/therapeutic use , Steroids/therapeutic use , Tomography, X-Ray Computed , Treatment Outcome , Virus Activation
19.
Bahrain Medical Bulletin. 2009; 31 (4): 178-183
in English | IMEMR | ID: emr-102566

ABSTRACT

Chronic hepatitis B virus [HBV] infection in renal patients could result from nosocomial transmission and outbreaks in dialysis units. Vaccination, universal precautions, regular virologic screening and segregation policy are important and effective control of HBV infection in hemodialysis unit. Chronic HBV infection poses problem to dialysis patients, their diagnosis, treatment of hepatic complications and pre-transplant management. This review summarizes the chronic HBV epidemiology, extrahepatic manifestations, management and prevention


Subject(s)
Humans , Hepatitis B/diagnosis , Hepatitis B/drug therapy , Hepatitis B/prevention & control , Kidney Failure, Chronic/virology , Renal Dialysis/adverse effects , Lamivudine , Kidney Transplantation , Hepatitis B, Chronic
20.
Acta méd. (Porto Alegre) ; 30: 538-551, 2009.
Article in Portuguese | LILACS | ID: lil-546772

ABSTRACT

As hepatites virais, principalmente as causadas pelos vírus A, B e C, são muito prevalentes no mundo inteiro. As formas crônicas das hepatites B e C são as mais comuns no nosso meio e acarretam importantes conseqüências, tanto sociais quanto econômicas . Sendo assim, é importante que o clínico, independente de sua área, saiba diagnosticar e encaminhar pacientes infectados. Este artigo tem como objetivo revisar os algoritmos diagnósticos das hepatites e expor os tratamentos atualmente preconizados para as formas crônicas destas afecções (hepatites B e C).


Subject(s)
Humans , Male , Female , Hepatitis A/diagnosis , Hepatitis A/drug therapy , Hepatitis B/diagnosis , Hepatitis B/drug therapy , Hepatitis C/diagnosis , Hepatitis C/drug therapy , Hepatitis, Chronic/diagnosis , Hepatitis, Chronic/drug therapy
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