Immunological Evaluation of Formulated Drugs against Typhoid

Authors

  • Syed S. Haque Indira Gandhi Institute of Medical Sciences - Clinical Biochemistry, Sheikhpura Sheikhpura, Patna, Bihar 800014

DOI:

https://doi.org/10.3889/oamjms.2014.069

Keywords:

Typhoid, Nitric oxide (NO), Delayed type of hypersensitivity (DTH), CMI

Abstract

OBJECTIVES: Typhoid fever an important causes of illness and death, particularly among children and adolescents in south-central and Southeast Asia, where enteric fever is associated with poor sanitation and unsafe food and water. Cell-mediated immunity (CMI) plays an important role for the survival of the host in experimental salmonellosis. Nitric oxide (NO) is the one of the product of macrophages activated by cytokines, microbial compounds or both, is derived from the amino acid L-arginine by the enzymatic activity of inducible nitric oxide synthase (iNOS or NOS2) which acts as antimicrobial molecule.

AIM: The aim was to examine the induction of DTH reaction in the animals treated with L-Arginine, ciprofloxacin and their combination followed by immunization with S. typhimurium cell lysate  as assessed by the footpad swelling test.

RESULTS: The results of the present study showed that the induction of DTH reaction in the animals treated with L-Arginine, ciprofloxacin and their combination followed by immunization with S. typhimurium cell lysate using an antigen revealed that the treatment with combination increased foot pad swelling significantly as compared to saline treated control animals at 48 hour which was followed by a decrease of the swelling at 72 hour.

CONCLUSIONS: Animal treated with L-arginine, ciprofloxacin and their combination showed increased cell mediated immune responses as evident by DTH response whereas groups (B+S) shows decreases CMI responses.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Plum Analytics Artifact Widget Block

References

Adamson GM, Billings RE. Cytokine toxicity and induction of NO synthase activity in cultured mouse hepatocytes. Toxicol Appl Pharmacol.1993;119: 100–107. DOI: https://doi.org/10.1006/taap.1993.1048

Granger D L, Jr. Hibbs JB, Perfect JR, Durack DT. Specific amino acid (L-arginine) requirement for the microbiostatic activity of murine macrophages. J Clin Invest. 1998;81:1129–1136. DOI: https://doi.org/10.1172/JCI113427

Nathan C. Nitric oxide as a secretory product of mammalian cells. FASEB J. 1992;6: 3051– 3064. DOI: https://doi.org/10.1096/fasebj.6.12.1381691

Palmer RMJ, Ferrige AG, Moncada S. Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor. Nature. 1987; 327: 524–526. DOI: https://doi.org/10.1038/327524a0

Setoguchi K, Takeya M, Akaike T, Suga M, Hattori R, Maeda H, Ando M, Takahashi K. Expression of inducible nitric oxide synthase and its involvement in pulmonary granulomatous inflammation of rats. Am J Pathol. 1996;149: 2005–2022.

Stueher DJ. Mammalian nitric oxide synthases. Adv Enzymol Relat Areas Mol Biol. 1992;65: 287–346. DOI: https://doi.org/10.1002/9780470123119.ch8

Sheffler LA, Wink DA, Melillo G, Cox GW. Exogenous nitric oxide regulates IFN-gamma plus lipopolysaccharide-induced nitric oxide synthase expression in mouse macrophages. J Immunol. 1995;155: 886–894.

Liles WC, Van Voorhis WC, Review, nomenclature and biologic significance of cytokines involved in inflammation and the host immune response. J Infect Dis. 1995;172:1573-1580. DOI: https://doi.org/10.1093/infdis/172.6.1573

Henderson B, Poole S, Wilson M. Bacterial modulins, a novel class of virulence factors which cause host tissue pathology by inducing cytokine synthesis. Microbiol Rev. 1996;60:316-341. DOI: https://doi.org/10.1128/MMBR.60.2.316-341.1996

Wilson M, Seymour R, Henderson B. Bacterial perturbation of cytokine networks. Infect Immun. 1998;66: 2401-2409. DOI: https://doi.org/10.1128/IAI.66.6.2401-2409.1998

Ciacci-Woolwine F, Blomfield, IC, Richardson, SH, Mizel SB. Salmonella flagellin induces tumor necrosis factor alpha in a human promonocytic cell line. Infect Immun. 1998;66: 1127-1134. DOI: https://doi.org/10.1128/IAI.66.3.1127-1134.1998

James SL. Role of nitric oxide in parasitic infections. Microbiol Rev. 1995; 59: 533–547. DOI: https://doi.org/10.1128/mr.59.4.533-547.1995

Liew FY, Millott S, Parkinson C, Palmer RMJ, Moncada S. Macrophage killing of Leishmania parasite in vivo is mediated by nitric oxide from L-arginine. J Immunol, 1990;144: 4794–4797.

Killar LM, Eisenstein TK. Immunity to Salmonella typhimurium infection in C3H/HeJ and C3H/HeNCrlBR mice: studies with an aromatic-dependent live S. typhimurium strains as a vaccine. Infect Immun. 1985;47: 605-612. DOI: https://doi.org/10.1128/iai.47.3.605-612.1985

Killar LM, Eisenstein TK. Differences in delayed-type hypersensitivity responses in various mouse strains in the C3H lineage infected with Salmonella typhimurium strain SL3235. J Immunol. 1984; 133: 1190-1196.

Mastroeni P, Villarreal Ramos B, Hormaeche CE. Role of T cells, TNF-a and IFN-y in recall of immunity to oral challenge with virulent salmonellae in mice vaccinated with live attenuated aro-Salmonella vaccines. Microb Pathog. 1992;13: 477-491. DOI: https://doi.org/10.1016/0882-4010(92)90014-F

Mackaness GB, Blanden RV, Collins FM. Host parasite relations in mouse typhoid. J Exp Med. 1966;124: 585-591. DOI: https://doi.org/10.1084/jem.124.4.585

Sztein MB, Wasserman SS, Tacket CO, Edelman R, Hone D, Lindberg AA, Levine MM. Cytokine production patterns and lymphoproliferative responses in volunteers orally immunized with attenuated vaccine strains of Salmonella typhi. J Infect Dis. 1994;170: 1508–1517. DOI: https://doi.org/10.1093/infdis/170.6.1508

Akeda H, Mitsuyama M, Tatsukawa K, Nomoto K, Takeya K. The synergistic contribution of macrophages and antibody to protection against Salmonella typhimurium during the early phase of infection. J Gen Microbiol. 1981; 123: 209-214. DOI: https://doi.org/10.1099/00221287-123-2-209

Tiwari H, Kamat PS. Cross-reactions in cell-mediated immunity to Salmonella enteric fever. J Med Microbiol. 1986;21: 233-237. DOI: https://doi.org/10.1099/00222615-21-3-233

Collins FM, Mackaness GB. Delayed hypersensitivity and Arthus reactivity in relation to host-resistance in Salmonella-infected mice. J Immunol. 1968;101: 830-845.

Ross R, Reske-Kunz AB. The role of NO in contact hypersensitivity. Int Immunopharmacol. 2001;1(8):1469-78. DOI: https://doi.org/10.1016/S1567-5769(01)00091-1

Bruch-Gerharz D, Ruzicka T, Kolb-Bachofen V. Nitric oxide in human skin: current status and future prospects. J Invest Dermatol. 1998; 110: 1 - 7. DOI: https://doi.org/10.1046/j.1523-1747.1998.00084.x

Downloads

Published

2014-09-15

How to Cite

1.
Haque SS. Immunological Evaluation of Formulated Drugs against Typhoid. Open Access Maced J Med Sci [Internet]. 2014 Sep. 15 [cited 2024 May 5];2(3):404-7. Available from: https://oamjms.eu/index.php/mjms/article/view/oamjms.2014.069

Issue

Section

A - Basic Science