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1.
Rev. cuba. invest. bioméd ; 40(1): e893, ene.-mar. 2021.
Artigo em Espanhol | LILACS, CUMED | ID: biblio-1289450

RESUMO

Introducción: El plasma de convalecientes es una inmunoterapia pasiva que se ha usado para el tratamiento y prevención de muchas enfermedades infecciosas por más de un siglo. Dada la falta de tratamiento específico para el nuevo coronavirus SARS-CoV-2, el plasma de convalecientes es una alternativa terapéutica potencial contra la COVID-19. Objetivo: Realizar una revisión del empleo del plasma de convalecientes como alternativa terapéutica a la COVID-19. Desarrollo: Se empleó la estrategia de búsqueda del tema; consultando las bases de datos Pubmed, SciELO, Lilacs, Cochrane Library y Web of Science. El plasma de convalecientes ha mostrado efectividad en el tratamiento de varias enfermedades virales. Así, la evidencia sobre su uso en los pacientes con COVID-19 es escasa, aunque se han obtenido resultados alentadores, pero no concluyentes por falta de un número mayor ensayos clínicos. Al mismo tiempo, Cuba incluye en sus protocolos de actuación contra la COVID-19 este tratamiento. Conclusiones: Esta alternativa resulta una herramienta inmunoterapéutica en los pacientes con la COVID-19, ya que mejora el estado clínico y disminuir la tasa de letalidad. Sin embargo, se necesitan más ensayos clínicos controlados y aleatorizados que afirmen su efectividad y seguridad(AU)


Introduction: Convalescent plasma is a form of passive immunotherapy which has been used for the treatment and prevention of many infectious diseases for more than one century. Given the absence of a specific treatment for the novel coronavirus SARS-CoV-2, convalescent plasma is a potential therapeutic alternative against COVID-19. Objective: Carry out a review about the use of convalescent plasma as a therapeutic alternative against COVID-19. Discussion: A search was conducted about the topic in the databases Pubmed, SciELO, Lilacs, Cochrane Library and Web of Science. Convalescent plasma has been shown to be effective in the treatment of several viral diseases. However, evidence of its use in COVID-19 patients is scant. Promising results have been obtained, though, but they are not conclusive due to the need of a larger number of clinical trials. In Cuba this treatment is included among the clinical management protocols for COVID-19. Conclusions: This alternative is an immunotherapeutic tool for the treatment of COVID-19 patients, since it improves their clinical status and reduces lethality rates. However, more controlled and randomized clinical trials are required confirming its effectiveness and safety(AU)


Assuntos
Humanos , Doenças Transmissíveis , Imunização Passiva , Coronavirus , Plasma/fisiologia
2.
Chinese Journal of Pharmacology and Toxicology ; (6): 87-94, 2016.
Artigo em Chinês | WPRIM | ID: wpr-488068

RESUMO

Cancer immunotherapies are recently gaining attention as viable therapeutic options. There are two types of immunotherapy:passive and active. The passive immunotherapies include several treatments such as monoclonal antibodies,either alone or as antibody-drug conjugates. The active immunotherapies include cancer vaccines which utilize the patient′s own cells as antigen presenting cells and target specific cancer antigens,and chimeric antigen receptor T-cell(CAR-T)therapy which engineers a patient′s T-cells to recognize cancer antigens through chimeric antigen receptors. Recent successes include the US FDA approval of a number of cancer immunotherapies such as treatments utilizing monoclonal antibodies against immune checkpoint inhibitors,the Provenge cancer vaccine that targets prostrate cancer,and a CAR-T against relapsed/refractory acute lymphoblastic leukemia that was designated with breakthrough drug status,all of which has had drug companies investigating cancer immunotherapies with intense enthusiasm. In this review we discuss where the field of immune-oncology stands today,highlight the latest findings and hypothesize future directions.

3.
Academic Journal of Second Military Medical University ; (12): 428-431, 2011.
Artigo em Chinês | WPRIM | ID: wpr-840087

RESUMO

Objective To observe the efficacy and safety of passive immunotherapy for treatment of renal transplant patients with severe pneumonia. Methods From August 2007 to October 2009, 51 patients with severe pneumonia following renal transplantation were treated with passive immunotherapy (thymosin and immunoglobulin), and they were taken as passive immunization group; and the other 52 patients with severe pneumonia following renal transplantation from January 2005 to July 2007 were taken as control group. The basic immunosuppressant was stopped and de-escalation therapy and broad-spectrum anti-infection therapy were given to both groups. Passive immunization group was given thymosin and immunoglobulin according to the patient condition. The peripheral CD4+ T-cell counts, clinical symptoms, signs and chest CT changes were observed in both groups. Results The survival rate of passive immunization group was significantly higher than that of control group (92. 2% vs 75.0%, P<0.05). The time of infection control in passive immunization group was significantly shorter than that of control group ([12.8±2.7] d vs [17.7±4.2] d, P<0.05). The length of hospital stay of the survivors was significantly shorter in passive immunization group than in the control group ([27.3 ± 7.0] d vs [36.3 ± 9.1] d, P<0.05). No acute rejection occurred in the passive immunization group, and 4 occurred in the control group. The CD4+ T-cell counts had an increasing tendency in the survivors of both groups and had a declining trend in those who finally died. Conclusion passive immunotherapy with thymosin andimmunoglobulin can improve the survival rate of renal transplant patients with severe pneumonia, and monitoring the variation of CD4+ T-cell counts may play an important role in guiding treatment and predicting prognosis.

4.
Journal of Veterinary Science ; : 43-46, 2006.
Artigo em Inglês | WPRIM | ID: wpr-36290

RESUMO

Infectious bursal disease (IBD) is an acute and highly contagious disease of young chickens caused by Birnavirus. Mortality of infected birds can be best prevented if injected with antibodies. The present study was an attempt to raise specific hyper-immune polyclonal antibodies against IBD virus in Pakistan. Commercial layers divided into four groups were injected with IBD vaccine subcutaneously according to four different treatment regimens. Eggs were collected daily and antibodies were purified from yolk with dextran sulphate. Titers of antibodies in serum and yolk were evaluated with enzyme linked immunosorbant assay and agar gel precipitation test. Antibody titers were significantly higher in yolk than serum. Eggs collected at 28 days post-vaccination had maximum antibody titers. Of treatment regimens, T3 was found to be most effective for hyperimmunization. Lyophilized antibodies stored at 4oC did not lose their activity till the end of experiment. IBD virus infected birds were injected with purified antibodies which induced 92% recovery as compared to control birds. The study implicates that the purified antibodies may be useful as a therapeutic agent to cure IBD infected birds.


Assuntos
Animais , Feminino , Anticorpos Antivirais/sangue , Infecções por Birnaviridae/imunologia , Galinhas , Gema de Ovo/imunologia , Ensaio de Imunoadsorção Enzimática/veterinária , Imunização/métodos , Imunoglobulinas/imunologia , Imunoterapia/métodos , Vírus da Doença Infecciosa da Bursa/imunologia , Doenças das Aves Domésticas/imunologia , Testes de Precipitina/veterinária , Vacinas Virais/imunologia
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