Literature DB >> 8559608

Antibodies to tumor necrosis factor-alpha: use as adjunctive therapy in established group B streptococcal disease in newborn rats.

L B Givner1, L Gray, T M O'Shea.   

Abstract

Group B Streptococcus (GBS) is the leading cause of neonatal sepsis. Adjunctive therapies are being sought to improve the outcome. Because increased blood levels of tumor necrosis factor (TNF)-alpha may play a role in the development of sepsis and an adverse outcome thereof, we evaluated the potential use of antibodies against TNF-alpha as adjunctive therapy of GBS sepsis. Using a neonatal rat model of GBS sepsis, we measured serum levels of TNF-alpha. Levels of TNF-alpha were significantly increased beginning 12 h after GBS inoculation and remained significantly increased at 30-36 h. We then examined the use of adjunctive therapy with antibody to TNF-alpha in animals with established GBS sepsis using polyclonal rabbit antirecombinant mouse TNF-alpha antiserum. Twelve hours after GBS inoculation, animals received a single dose of antibody to TNF-alpha or normal rabbit serum, and penicillin therapy (twice a day for 3 d) was begun. Animals receiving penicillin and antibody to TNF-alpha had a survival rate of 52% (13 of 25) versus 29% (7 of 24) for animals receiving penicillin and normal rabbit serum. Thus, the use of antibodies directed against TNF-alpha may have a role as adjunctive therapy of established GBS sepsis in the newborn infant.

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Year:  1995        PMID: 8559608     DOI: 10.1203/00006450-199510000-00013

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  8 in total

1.  Human monocyte receptors involved in tumor necrosis factor responses to group B streptococcal products.

Authors:  M Cuzzola; G Mancuso; C Beninati; C Biondo; C von Hunolstein; G Orefici; T Espevik; T H Flo; G Teti
Journal:  Infect Immun       Date:  2000-02       Impact factor: 3.441

2.  Endotoxin-induced lethality in neonatal mice is counteracted by interleukin-10 (IL-10) and exacerbated by anti-IL-10.

Authors:  F Nicoletti; G Mancuso; F A Ciliberti; C Beninati; M Carbone; S Franco; V Cusumano
Journal:  Clin Diagn Lab Immunol       Date:  1997-09

3.  Group B Streptococci Induce Proinflammatory Responses via a Protein Kinase D1-Dependent Pathway.

Authors:  Kirtikumar Upadhyay; Jeoung-Eun Park; Tae Won Yoon; Priyanka Halder; Young-In Kim; Victoria Metcalfe; Ajay J Talati; B Keith English; Ae-Kyung Yi
Journal:  J Immunol       Date:  2017-05-01       Impact factor: 5.422

4.  Roles of the bacterial cell wall and capsule in induction of tumor necrosis factor alpha by type III group B streptococci.

Authors:  J G Vallejo; C J Baker; M S Edwards
Journal:  Infect Immun       Date:  1996-12       Impact factor: 3.441

5.  Interleukin-18 is an essential element in host resistance to experimental group B streptococcal disease in neonates.

Authors:  Vitaliano Cusumano; Angelina Midiri; Valentina Valeria Cusumano; Antonella Bellantoni; Giuseppe De Sossi; Giuseppe Teti; Concetta Beninati; Giuseppe Mancuso
Journal:  Infect Immun       Date:  2004-01       Impact factor: 3.441

6.  Mesenteric lymph duct drainage attenuates acute lung injury in rats with severe intraperitoneal infection.

Authors:  Yanmin Zhang; Shukun Zhang; Naiqiang Tsui
Journal:  Inflammation       Date:  2015       Impact factor: 4.092

7.  Translational research in sepsis - an ultimate challenge?

Authors:  Tim G Kampmeier; Christian Ertmer; Sebastian Rehberg
Journal:  Exp Transl Stroke Med       Date:  2011-11-14

8.  The β-hemolysin and intracellular survival of Streptococcus agalactiae in human macrophages.

Authors:  Anubha Sagar; Carolin Klemm; Lara Hartjes; Stefanie Mauerer; Ger van Zandbergen; Barbara Spellerberg
Journal:  PLoS One       Date:  2013-04-04       Impact factor: 3.240

  8 in total

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