• Users Online: 23
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 


 
 Table of Contents  
ORIGINAL ARTICLE
Year : 2016  |  Volume : 16  |  Issue : 1  |  Page : 6-9

Cytokines responses to human African trypanosomiasis infection in Abraka, Nigeria


1 Department of Zoology, Ambrose Alli University, Ekpoma, Nigeria
2 Department of Medical Microbiology and Parasitology, College of Health Sciences, Delta State University, Abraka, Nigeria

Date of Web Publication8-Sep-2016

Correspondence Address:
C Isaac
Department of Zoology, Ambrose Alli University, Ekpoma
Nigeria
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1596-4078.189972

Rights and Permissions
  Abstract 

Background: The staging of human African trypanosomiasis (HAT) has been greeted with different benchmarks ranging from white blood cell counts to the use of immune component profiles across regions.
Objective: The aim of this study was to analyze an array of cytokines to identify potential markers that could be used in the staging of HAT in Nigeria.
Methods: Sera and cerebrospinal fluid (CSF) of 35 HAT seropositives from Abraka, Delta State, Nigeria were subjected to cytokines (interleukin-10 [IL-10], tumor necrosis factor-α, IL-1α, IL-7, and IL-13) analysis using enzyme-linked immunosorbent assay. Welch t-test and Tukey analysis of variance were used to analyze the data.
Results: Comparing mean cytokine levels of weakly, moderately, and strongly positives and between as early and late stages results showed significantly depressed CSF levels of IL-1α and IL-7 while IL-10 was significantly elevated in the strongly positives as well as in the late stage.
Conclusion: We strongly suggest that IL-10 could be playing a key role in the immuno-pathology of HAT, thus should be considered a biomarker for the late stage.

Keywords: Cytokines, human African trypanosomiasis, late stage, Nigeria


How to cite this article:
Isaac C, Nmorsi O, Igbinosa I B. Cytokines responses to human African trypanosomiasis infection in Abraka, Nigeria. Niger J Health Sci 2016;16:6-9

How to cite this URL:
Isaac C, Nmorsi O, Igbinosa I B. Cytokines responses to human African trypanosomiasis infection in Abraka, Nigeria. Niger J Health Sci [serial online] 2016 [cited 2017 Apr 28];16:6-9. Available from: http://www.chs-journal.com/text.asp?2016/16/1/6/189972


  Introduction Top


Human African trypanosomiasis (HAT) is caused by the subspecies of Trypanosoma brucei vectored by Glossina. After infective bite, parasites initially proliferate in the hemolymphatic system (first stage); and as the disease progresses, the central nervous system (CNS) is invaded (second stage). However, because of the difficulty in the identification of parasites in the cerebrospinal fluid (CSF), it has been recommended that counts of white blood cells (WBCs) could be used in staging HAT [1] because incorrect staging of HAT could lead to complications from inappropriate application of therapy. However, the use of CSF WBCs counts have been challenged as different endemic regions have reported varied benchmarks. [2],[3],[4] Hence, the quest to using components of the immune system in the staging of HAT should be explored since the control of African trypanosomiasis (AT) partly requires the signaling of immune cells by cytokines. [5],[6]

Cytokines orchestrate a Type I and/or a Type II immune response(s) that plays a role in AT disease outcomes. [6],[7],[8],[9],[10] Trypanosome-derived products activates the generation of pro-inflammatory mediators (interleukin-alpha [IL-1α] and tumor necrosis factor-alpha [TNF-α]); [11] and it has been proposed to be part of the immune process leading to the pathological conditions of HAT. [12],[13] Similarly, IL-7, a Type I cytokine-triggered the production of IL-1α and TNF-α that reportedly influenced disease outcome. [14] TNF-α has been implicated in the dysfunction of the blood-brain-barrier, enabling entry of trypanosomes into the CNS and thus initiating late stage of infection. [15]

IL-10, a Type II cytokine has been suggested to be a critical immunomodulator of HAT such that it down-regulates a range of inflammatory and activation markers on macrophages including TNF-α. [16] However, up-regulation of TNF-α by IL-10 in T. brucei gambiense-infected patients has been demonstrated. [12] The role of Type II cytokines (IL-10 and IL-13) in conferring immunity to HAT positives is highly speculative because of the contrasting reports by authors who have advanced deleterious, [17] protective, [9] or null effects. [18]

In addition, data from Uganda and Malawi have shown differences in TNF-α profile of HAT patients with early and late stages of infection. [19] In the middle of these varied suggestions regarding the roles of some cytokines in HAT disease progression, it was imperative we described for our locality. Thus, the roles of IL-10, TNF-α, IL-α, IL-7, and IL-13 among seropositives as well in the early and late stages of HAT are discussed.


  Materials and Methods Top


Study area

Volunteers were drawn from three communities (Umeghe, Urhouka and Ugono) of Abraka, a HAT endemic focus. Abraka which is in Delta State, Nigeria lies between latitude 5°47' to 6°15'N and longitude 5°42' to 6E. The predominant occupation of the over 5000 population is farming.

Ethical considerations

Ethical permission was obtained from the Delta State Ministry of Health and Eku Baptist Hospital. Informed consents were sought and granted by participants.

Staging human African trypanosomiasis

Of the 474 screened using card agglutination tests for trypanosomiasis, only 35 were recruited into the study being seropositive as well as measured up to the inclusion criteria. The demographics of the 35 positives are thus: 20 females and 15 males; age group ranged between 7 and 70 years with the following breakdown (7-10 years [n = 5], 11-18 years [n = 14], 19-50 years [n = 13] and 51-70 years [n = 3]). Double serial dilution were used to group seropositives into: Weak (1:2-1:4) (n = 9), moderate (1:8-1:16) (n = 12), and strong (≥1:32). [14] In addition, the 35 seropositives were further screened for parasites in the blood and CSF including determining the counts of white blood cells in the CSF. So, 16 persons were either at the early (n = 12) or late stage (n = 4) of HAT. [1] Following medical examinations, most of the seropositives had symptoms such as malaise, anemia, headache, pyrexia, weight loss, and weakness.

Exclusion criteria

We excluded volunteers with malaria particularly those with moderate/heavy parasite load including individuals showing symptoms of malaria. Similarly, individuals with overt diseases such as viral hepatitis B, HIV, sickle cell anemia, and diabetes were identified using standard procedures and excluded.

Cytokine assay

Sera and CSF were obtained from the positives and then analyzed for IL-10, TNF-α, IL-1α, IL-7, and IL-13 using standard enzyme-linked immunosorbent assay according to the manufacture's protocol (Abcam Plc, United Kingdom). Similarly, cytokine analysis was carried out on 20 control subjects who were HAT negative among the population.

Statistical analysis

Data obtained were subjected to the test instruments of Welch t-test and Tukey analysis of variance using InStat Graphpad Statistical Package, Inc., (CA 92037, USA).


  Results Top


[Table 1] shows the distribution of cytokine levels in relation to seropositive status. The mean level of IL-10 in the strongly positive was highly elevated (P < 0.0001). Similarly, mean TNF-α for strongly positive was relatively high (P < 0.001). Other cytokines (IL-1α, IL-7, and IL-13) were not significant with the degree of positivity.
Table I: Cytokine levels of seropositive and negative volunteers

Click here to view


[Table 2] compares the cytokine levels between early and late stages of HAT. Late stage of HAT for mean IL-10 was significantly elevated in the serum and the CSF. Raised mean levels were only observed in TNF-α in the serum of late stage, but in the CSF, no significant change was seen. Meanwhile, CSF IL-1α and IL-7 were significantly depressed in the late stage (P < 0.05). For IL-13, no change was recorded both in the serum and in the CSF (P > 0.05). However, our results should be viewed with caution because of the small sample sizes for individuals at the early (n = 12) and late (n = 4) stages.
Table II: Cytokine levels in early and late stages of human African trypanosomiasis

Click here to view



  Discussion Top


High levels of IL-10 are associated with protection of CNS from inflammatory pathology particularly at the point when parasites first enter the brain. [20] Our result on serum IL-10 in the strongly positives and late stage of HAT corroborates the findings of Sternberg et al. [21] IL-10 is known to facilitate the proliferation, differentiation, and immunoglobulin secretion processes of B-cells. [3],[22] Furthermore, raised IL-10 response has been ascribed to antigen inhibition properties. [23]

An in vitro study has implicated TNF-α as a growth control factor of T. b. gambiense in the midst of increased number and lifespan. [24] Thus suggesting that raised TNF-α could be conferring some form of protection to T. b. gambiense-infected individuals as this may be the case in the seropositives as well as in the serum of late stage. However, no change was seen in the CSF of the late and early HAT patients. Impaired secretion of TNF-α by macrophages has been associated with an increased expression of anti-inflammatory cytokines. [19] The interplay between pro- and anti-inflammatory cytokines could be the case here as it has been evidently argued that IL-10 could modulate. [16] We are therefore of the view that this likely interaction could be the narrative for CSF TNF-α being a possible attempt to ameliorating neuropathological conditions. [19],[20] Similarly, the suppressed levels of CSF IL-1α and IL-7 could be the effect of the activity of other anti-inflammatory cytokines following infection. [16]

In this study, only IL-13 was unaltered among seropositives and between late and early stages of HAT in the serum and CSF. This is quite instructive in the sense that it shows noninvolvement in the immunopathology of HAT. In support of this, the data on mice suggested that IL-13 were not the main trigger of alternative macrophages because IL-13 signaling occurred independently of an anti-inflammatory cytokine (IL-4), thereby corroborating the natural propensity of animals to develop alternatively activated macrophages. [10],[25]


  Conclusion Top


It is evident that IL-10, TNF-α, IL-α, and IL-7 are interacting in a complex manner with itself and others in boosting immunity of HAT patients. However, prominent among these cytokines is IL-10 being raised in seropositives as well as in serum and CSF of late stage of HAT. We thus suggest that IL-10 should be considered in the staging of HAT as it has proved to be a potential biomarker.

Acknowledgments

We would like to thank all the HAT positive volunteers.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
  References Top

1.
World Health Organisation. Control and Surveillance of African Trypanosomiasis. Geneva, Switzerland: World Health Organisation; 1998.  Back to cited text no. 1
    
2.
Bisser S, Bouteille B, Sarda J, Stanghellini A, Ricard D, Jauberteau MO, et al. Contribution of biochemical tests in the diagnosis of the nervous phase of human African trypanosomiasis. Bull Soc Pathol Exot 1997;90:321-6.  Back to cited text no. 2
[PUBMED]    
3.
Lejon V, Reiber H, Legros D, Djé N, Magnus E, Wouters I, et al. Intrathecal immune response pattern for improved diagnosis of central nervous system involvement in trypanosomiasis. J Infect Dis 2003;187:1475-83.  Back to cited text no. 3
    
4.
Miezan TW, Meda HA, Doua F, Yapo FB, Baltz T. Assessment of central nervous system involvement in gambiense trypanosomiasis: Value of the cerebro-spinal white cell count. Trop Med Int Health 1998;3:571-5.  Back to cited text no. 4
[PUBMED]    
5.
Dempsey WL, Mansfield JM. Lymphocyte function in experimental African trypanosomiasis. V. Role of antibody and the mononuclear phagocyte system in variant-specific immunity. J Immunol 1983;130:405-11.  Back to cited text no. 5
    
6.
Kaushik RS, Uzonna JE, Gordon JR, Tabel H. Innate resistance to Trypanosoma congolense infections: Differential production of nitric oxide by macrophages from susceptible BALB/c and resistant C57Bl/6 mice. Exp Parasitol 1999;92:131-43.  Back to cited text no. 6
[PUBMED]    
7.
Sileghem M, Darji A, Hamers R, De Baetselier P. Modulation of IL-1α production and IL-1α release during experimental trypanosome infections. Immunology 1989;68:137-9.  Back to cited text no. 7
[PUBMED]    
8.
Fonseca SG, Reis MM, Coelho V, Nogueira LG, Monteiro SM, Mairena EC, et al. Locally produced survival cytokines IL-15 and IL-7 may be associated to the predominance of CD8+T cells at heart lesions of human chronic chagas disease cardiomyopathy. Scand J Immunol 2007;66:362-71.  Back to cited text no. 8
[PUBMED]    
9.
Bakhiet M, Jansson L, Büscher P, Holmdahl R, Kristensson K, Olsson T. Control of parasitemia and survival during Trypanosoma brucei brucei infection is related to strain-dependent ability to produce IL-4. J Immunol 1996;157:3518-26.  Back to cited text no. 9
    
10.
Noël W, Hassanzadeh G, Raes G, Namangala B, Daems I, Brys L, et al. Infection stage-dependent modulation of macrophage activation in Trypanosoma congolense-resistant and -susceptible mice. Infect Immun 2002;70:6180-7.  Back to cited text no. 10
    
11.
Tachado SD, Schofield L. Glycosylphatidylinositol toxin of Trypanosoma brucei regulates IL-α and TNF-α expressions in macrophages by protein tyrosine kinase-mediated signal transduction. Biochem Biophys Res Commun 1994;205:984-91.  Back to cited text no. 11
    
12.
Rhind SG, Sabiston BH, Shek PN, Buguet A, Muanga G, Stanghellini A, et al. Effect of melarsoprol treatment on circulating IL-10 and TNF-α levels in human African trypanosomiasis. Clin Immunol Immunopathol 1997;83:185-9.  Back to cited text no. 12
    
13.
Okomo-Assoumou MC, Daulouede S, Lemesre JL, N'Zila-Mouanda A, Vincendeau P. Correlation of high serum levels of tumor necrosis factor-α with disease severity in human African trypanosomiasis. Am J Trop Med Hyg 1995;53:539-43.  Back to cited text no. 13
[PUBMED]    
14.
Weitzmann NM, Cenci S, Ritas L, Brown C, Pacifici RC. Interleukin-7 stimulates osteoclastogenic formation by up-regulating T-cell production of soluble osteoclastogenic cytokines. Immunobiology 2000;96:1873-8.  Back to cited text no. 14
    
15.
Enanga B, Burchmore RJ, Stewart ML, Barrett MP. Sleeping sickness and the brain. Cell Mol Life Sci 2002;59:845-58.  Back to cited text no. 15
[PUBMED]    
16.
de Waal Malafyt R, Moore KW. Interleukin-10. In: Thompson AW, editor. The Cytokine Handbook. 3 rd ed. San Diego: Academic Press; 1998. p. 333-64.  Back to cited text no. 16
    
17.
Uzonna JE, Kaushik RS, Gordon JR, Tabel H. Immunoregulation in experimental murine Trypanosoma congolense infection: Anti-IL-10 antibodies reverse trypanosome-mediated suppression of lymphocyte proliferation in vitro and moderately prolong the lifespan of genetically susceptible BALB/c mice. Parasite Immunol 1998;20:293-302.  Back to cited text no. 17
[PUBMED]    
18.
Schopf LR, Filutowicz H, Bi XJ, Mansfield JM. Interleukin-4-dependent immunoglobulin G1 isotype switch in the presence of a polarized antigen-specific Th1-cell response to the trypanosome variant surface glycoprotein. Infect Immun 1998;66:451-61.  Back to cited text no. 18
[PUBMED]    
19.
MacLean L, Chisi JE, Odiit M, Gibson CW, Ferris KP, Sternberg MJ. Severity of human African trypanosomiasis in East Africa is associated with geographical location, parasite genotype, and host inflammatory cytokine response profile. Infect Immun 2004;72:7040-4.  Back to cited text no. 19
    
20.
Sternberg JM, Rodgers J, Bradley B, Maclean L, Murray M, Kennedy PG. Meningoencephalitic African trypanosomiasis: Brain IL-10 and IL-6 are associated with protection from neuro-inflammatory pathology. J Neuroimmunol 2005;167:81-9.  Back to cited text no. 20
[PUBMED]    
21.
Lejon V, Lardon J, Kenis G, Pinoges L, Legros D, Bisser S, et al. Interleukin (IL)-6, IL-8 and IL-10 in serum and CSF of Trypanosoma brucei gambiense sleeping sickness patients before and after treatment. Trans R Soc Trop Med Hyg 2002;96:329-33.  Back to cited text no. 21
[PUBMED]    
22.
Guzman J, Frei K, Nadal D. In vitro immunization: Generation of neutralizing monoclonal antibodies to human interleukin-10. J Immunol Methods 1995;179:265-8.  Back to cited text no. 22
[PUBMED]    
23.
Namangala B, Brys L, Magez S, De Baetselier P, Beschin A. Trypanosoma brucei brucei infection impairs MHC class II antigen presentation capacity of macrophages. Parasite Immunol 2000;22:361-70.  Back to cited text no. 23
[PUBMED]    
24.
Daulouède S, Bouteille B, Moynet D, De Baetselier P, Courtois P, Lemesre JL, et al. Human macrophage tumor necrosis factor (TNF)-alpha production induced by Trypanosoma brucei gambiense and the role of TNF-alpha in parasite control. J Infect Dis 2001;183:988-91.  Back to cited text no. 24
    
25.
Mills CD, Kincaid K, Alt JM, Heilman MJ, Hill AM. M-1/M-2 macrophages and the Th1/Th2 paradigm. J Immunol 2000;164:6166-73.  Back to cited text no. 25
    



 
 
    Tables

  [Table 1], [Table 2]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
Introduction
Materials and Me...
Results
Discussion
Conclusion
References
Article Tables

 Article Access Statistics
    Viewed399    
    Printed28    
    Emailed0    
    PDF Downloaded8    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]