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Research Article | Open Access

Effect of Antimonial Therapy on Levels of (TNF-α and IL-1β) Cytokines in Cutaneous Leishmaniasis Patients in Iraq

Hasan Raheem Khudhur1( )Ahmed Abbas Hasan2Rawaa Adday Ali3
Ministry of Education, Iraq
College of Health and Medical Techniques, Kufa, Al-Furat Al-Awsat Technical University, 31003 Al-Kufa, Iraq
AL-Qasim Green University, College of Veterinary Medicine, Microbiology Department, Iraq
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Abstract

This study aimed to study the effective antimonial therapy on circulating levels proinflammatory cytokines, and their effect on susceptibility to cutaneous leishmaniasis (CL) infection in the Iraqi population. Fifty CssL patients were treated with pentavalent antimonial salts (pentostam) for 7 weeks. Leishmania species were identified by Nested-Polymerase chain reaction method, and in all the cases the strains corresponded to Leishmania major. Circulating plasma levels of the proinflammatory cytokines interleukin-1 and tumor necrosis factor-alpha were determined for CL patients and healthy subjects before and during 7 weeks after the treatment were started. Concentrations were detected by enzyme-linked immunosorbent assay technique using a quantitative sandwich enzyme immunoassay technique. Proinflammatory cytokines significantly increased after 7 days postinfection compared to levels in the pretreatment patients. It was clearly recorded in the present study that the level of interleukin-1 and tumor necrosis factor-alpha in the serum of CL patients was responsively increasing with the antimonial therapy dose.

References

[1]

S. Ahmed, M. Colmenares, L. Soong, et al., Intradermal infection model for pathogenesis and vaccine studies of murine visceral leishmaniasis. Infection and Immunity, 2003, 71(1): 401-410.

[2]

J. Blum, P. Desjeux, E. Schwartz, et al., Treatment of cutaneous leishmaniasis among travellers. Journal of Antimicrobial Chemotherapy, 2004, 53(2): 158-166.

[3]

P. Desjeux, Worldwide increasing risk factors for leishmaniasis. Medical Microbiology and Immunology, 2001, 190(1-2): 77-79.

[4]

J. Gonzalez, Baghdad boil festers as new enemy of GIs. New York Daily, 2003.

[5]

B.J. Holaday, M.M. de Lima Pompeu, T. Evans, et al., Correlates of Leishmania-specific immunity in the clinical spectrum of infection with Leishmania chagasi. Journal of Infectious Diseases, 1993, 167(2): 411-417.

[6]

R.G. Titus, B. Sherry, and A. Cerami, Tumor necrosis factor plays a protective role in experimental murine cutaneous leishmaniasis. Journal of Experimental Medicine, 1989, 170(6): 2097-2104.

[7]

G.B. Alomashi, H.R. Khudhur, NRAMP1 gene polymorphism and susceptibility to cutaneous leishmaniasis in Iraq. Nano Biomed. Eng, 2017, 9(4): 333-336.

[8]

R. Birnbaum, N. Craft, Innate immunity and Leishmania vaccination strategies. Dermatologic clinics, 2011, 29(1): 89-102.

[9]
R. Locksley, F. Heinzel, M. Sadick, et al. Murine cutaneous leishmaniasis: susceptibility correlates with differential expansion of helper T-cell subsets. Annales de l'Institut Pasteur/Immunologie. Elsevier, 1987.
[10]

F. Liew, Y. Li, and S. Millott, Tumour necrosis factor (TNF-alpha) in leishmaniasis. Ⅱ. TNF-alpha-induced macrophage leishmanicidal activity is mediated by nitric oxide from L-arginine. Immunology, 1990, 71(4): 556.

[11]

M. Belosevic, C. Davis, M. Meltzer, et al., Regulation of activated macrophage antimicrobial activities. Identification of lymphokines that cooperate with IFN-gamma for induction of resistance to infection. The Journal of Immunology, 1988, 141(3): 890-896.

[12]

D. Santos, T.M. Campos, M. Saldanha, et al., IL-1β production by intermediate monocytes is associated with immunopathology in cutaneous leishmaniasis. Journal of Investigative Dermatology, 2018, 138(5): 1107-1115.

[13]

J. Kim, S. Amar, Periodontal disease and systemic conditions: A bidirectional relationship. Odontology, 2006, 94(1): 10-21.

[14]

M.G. Netea, A. Simon, F. van de Veerdonk, et al., IL-1β processing in host defense: Beyond the inflammasomes. PLoS Pathogens, 2010, 6(2): e1000661.

[15]

R. Silvestre, A. Cordeiro-da-Silva, and A. Ouaissi, Live attenuated Leishmania vaccines: a potential strategic alternative. Archivum Immunologiae et Therapiae Experimentalis, 2008, 56(2): 123-126.

[16]

J. Berman, Recent developments in leishmaniasis: Epidemiology, diagnosis, and treatment. Current Infectious Disease Reports, 2005, 7(1): 33-38.

[17]

D.O. Santos, C.E. Coutinho, M.F. Madeira, et al., Leishmaniasis treatment -a challenge that remains: A review. Parasitology Research, 2008, 103(1): 1-10.

[18]

P. van Thiel, T. Leenstra, P. Kager, et al., Miltefosine treatment of Leishmania major infection: an observational study involving Dutch military personnel returning from northern Afghanistan. Clinical Infectious Diseases, 2010, 50(1): 80-83.

[19]

S.L. Croft, V. Yardley, Chemotherapy of leishmaniasis. Current Pharmaceutical Design, 2002, 8(4): 319-342.

[20]
B. Herwaldt, A. Magill, Chapter 5 Leishmaniasis, cutaneous. Yellow Book. CDC Travelers' Health, 2010.
[21]

M. Ouellette, J. Drummelsmith, and B. Papadopoulou, Leishmaniasis: Drugs in the clinic, resistance and new developments. Drug Resistance Updates, 2004, 7(4): 257-266.

[22]

M. Ibrahim, M. Hag-Ali, A. El-Hassan, et al., Leishmania resistant to sodium stibogluconate: drug-associated macrophage-dependent killing. Parasitology Research, 1994, 80(7): 569-574.

[23]

B. Berger, A. Fairlamb, Interactions between immunity and chemotherapy in the treatment of the trypanosomiases and leishmaniases. Parasitology, 1992, 105(S1): S71-S78.

[24]

L.R. Brunet, Nitric oxide in parasitic infections. International Immunopharmacology, 2001, 1(8): 1457-1467.

[25]

H. Murray, M. Oca, A. Granger, et al., Requirement for T cells and effect of lymphokines in successful chemotherapy for an intracellular infection. Experimental visceral leishmaniasis. The Journal of Clinical Investigation, 1989, 83(4): 1253-1257.

[26]

S. Rais, A. Perianin, M. Lenoir, et al., Sodium stibogluconate (Pentostam) potentiates oxidant production in murine visceral leishmaniasis and in human blood. Antimicrobial Agents and Chemotherapy, 2000, 44(9): 2406-2410.

[27]

A.M. Da-Cruz, R. Bittar, M. Mattos, et al., T-cell-mediated immune responses in patients with cutaneous or mucosal leishmaniasis: Long-term evaluation after therapy. Clin. Diagn. Lab. Immunol. , 2002, 9(2): 251-256.

[28]

A. Kocyigit, S. Gur, M.S. Gurel, et al., Antimonial therapy induces circulating proinflammatory cytokines in patients with cutaneous leishmaniasis. Infection and Immunity, 2002, 70(12): 6589-6591.

[29]

R.C. Team, R foundation for statistical computing; Vienna, Austria: 2014. R: A Language and Environment for Statistical Computing, 2015: 2013.

[30]
H. Arroub, A. Alaoui, and K. Habbari, Etude eco-epidemiologique de la leishmaniose cutanée dans la région de Foum Jamâa (Azilal, Maroc). Le Premier Colloque International sur les Changements Climatiques et Environnement. Faculté des Sciences, Rabat, Maroco. 2010.
[31]
E. Sarhan, Study on epidemiology of cutaneous leishmaniasis in Baghdad. MSc Thesis submitted to College of Medicine, University of Baghdad, 1998.
[32]
A.M. Mahmood, Immunological evaluation of zinc concentration in cutaneous leishmania patients in Al-Haweja district. M. SC. Thesis, College of Medicine, University of Tikrit, 2006.
[33]
H. Al-Mayale, The evaluation and using of some of immunological tests in epidemiological study of leishmaniasis in Al-Qadisia province. Thesis of Doctorate of Philosophy in Zoology–Parasitology, University of AL-Qadisiya, 2004.
[34]
A.F. Al-Jeboori, Study of some epidemiological, histopathological and hematological of cutaneous leishmaniasis in Al-Diwaniya Governorate. MSc. Thesis, Al-Qadisiya University, 2014.
[35]

A.M. Al-Samarai, H.S. Al-Obaidi, Cutaneous leishmaniasis in Iraq. The Journal of Infection in Developing Countries, 2009, 3(02): 123-129.

[36]

I. Sharifi, A. Fekri, M. Aflatonian, et al., Cutaneous leishmaniasis in primary school children in the south-western Iranian city of Bam, 1994-95. Bulletin of the World Health Organization, 1998, 76(3): 289.

[37]

Z.M.P. Luz, A.R.D. Silva, F.D.O. Silva, et al., Lesion aspirate culture for the diagnosis and isolation of Leishmania spp. from patients with cutaneous leishmaniasis. Memorias do Instituto Oswaldo Cruz, 2009, 104(1): 62-66.

[38]

I.K. Al-Aubaidi, Serum cytokine production in patients with cutaneous leishmaniasis before and after treatment. Iraqi Journal of Medical Sciences, 2011, 9(1).

[39]

A. Sodhi, K. Pai, R.K. Singh, et al., Activation of human NK cells and monocytes with cisplatin in vitro. International Journal of Immunopharmacology, 1990, 12(8): 893-898.

[40]

H.R. Khudhur, G.B. Alomashi, Effect of NRAMP1 gene polymorphism on levels of (TNF-α1and IL-1β) cytokines in cutaneous Leishmaniasis patients in Iraq. Journal of Immunology and Clinical Microbiology, 2018, 3(2).

[41]

S.J. Green, R. Crawford, J. Hockmeyer, et al., Leishmania major amastigotes initiate the L-arginine-dependent killing mechanism in IFN-gamma-stimulated macrophages by induction of tumor necrosis factor-alpha. The Journal of Immunology, 1990, 145(12): 4290-4297.

[42]

L. Akman, H. Aksu, R.Q. Wang, et al., Multi-site DNA polymorphism analyses of Leishmania isolates define their genotypes predicting clinical epidemiology of leishmaniasis in a specific region. Journal of Eukaryotic Microbiology, 2000, 47(6): 545-554.

[43]

W.L. Roberts, P.M. Rainey, Antileishmanial activity of sodium stibogluconate fractions. Antimicrobial Agents and Chemotherapy, 1993, 37(9): 1842-1846.

[44]

A.M. Beebe, S. Mauze, N.J. Schork, et al., Serial backcross mapping of multiple loci associated with resistance to Leishmania major in mice. Immunity, 1997, 6(5): 551-557.

[45]

M. García, L. Monzote, A.M. Montalvo, et al., Screening of medicinal plants against Leishmania amazonensis. Pharmaceutical Biology, 2010, 48(9): 1053-1058.

[46]

H. Murray, M. Oca, A. Granger, et al., Requirement for T cells and effect of lymphokines in successful chemotherapy for an intracellular infection. Experimental visceral leishmaniasis. Journal of Clinical Investigation, 1989, 83(4): 1253.

[47]

S. Sodhi, N. Ganguly, N. Malla, et al., Effect of sodium stibogluconate on the status of interleukin-I production in normal & Leishmania donovani infected BALB/c mice. The Indian Journal of Medical Research, 1990, 91: 344-348.

Nano Biomedicine and Engineering
Pages 340-346
Cite this article:
Khudhur HR, Hasan AA, Ali RA. Effect of Antimonial Therapy on Levels of (TNF-α and IL-1β) Cytokines in Cutaneous Leishmaniasis Patients in Iraq. Nano Biomedicine and Engineering, 2019, 11(4): 340-346. https://doi.org/10.5101/nbe.v11i4.p340-346

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Received: 25 July 2019
Accepted: 11 November 2019
Published: 11 November 2019
© Hasan Raheem Khudhur, Ahmed Abbas Hasan, and Rawaa Adday Ali.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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