American Journal of Biomedical and Life Sciences
Volume 3, Issue 4-1, July 2015, Pages: 13-16

Oral Mucosal Tolerance Versus Systemic Immune Response to Salmonella typhi Antigen

Ibrahim Mohamed Saeed Shnawa1, Zainab Khudhur Ahmed Al-Mahdi2

1College of Biotechnology, Al-Kasim University, Babylon Province, Iraq

2Medical Science Department, College of Nursing, Babylon University, Babylon Province, Iraq

Email address:

(I. M. S. Shnawa)

To cite this article:

Ibrahim Mohamed Saeed Shnawa, Zainab Khudhur Ahmed Al-Mahdi. Oral Mucosal Tolerance Versus Systemic Immune Response to Salmonella typhi Antigen. American Journal of Biomedical and Life Sciences. Special Issue: Advances in Oral Immunity. Vol. 3, No. 4-1, 2015, pp. 13-16. doi: 10.11648/j.ajbls.s.2015030401.15


Abstract: It was demonstrated that the oral vaccine application of Salmonella typhi antigen can activate low antibody agglutinin titer (mean:40±0) comparing with high agglutination titer induced by Intramuscular administration  of Salmonella typhi antigen (mean 560.0 ± 51.64) as well as anti-Salmonella typhi IgG ELIZA shows high mean index value(mean = 0.6957±0.10) comparing with the low index value  induced by oral rout were (mean= 0.028±0.014) while anti Salmonella typhi IgM ELIZA test show mean index value = 0.6339±0.0385 comparing with low IgM index value (mean= 0.1560±0.070) induced by oral rout (Rsquared 0.7457, t test 3.3. The pro –inflammatory cytokines IL-1α was high in intramuscular rout 217.089±39.78 than its concentration with in oral administrated group (100.4±12.09), IL-12  was about  the same concentration both in oral rout and intramuscular rout subsequently (23.607 and 23.17) p value 0.01, R squared (0.3958).However the immune responses were  not absolutely absent in the oral administrated group, this reflect the fact that there is a selectivity in taking oral antigens from digestive mucosal surfaces but this immune feature and selectivity theme  may vary from antigen to another. In conclusion the recent and ongoing expansion of  a new information about the mucosal and  systemic immune responses lend a promise to provide the tools needed to exploit the full potential and development of both mucosal and intramuscular vaccines.

Keywords: Oral Tolerance, Systemic Immune Response, Intramuscular Rout


1. Introduction

Many vaccines and antigens that are given orally or deposited directly on mucosal surface ,will face the same gauntlet of host defenses as do microbial pathogens[1] .Such vaccine and antigens are being diluted in mucosal secretion, captured in mucus gels, attacked by proteases and nucleases and excluded by epithelial barriers[2,3] . Thus the exact dose of mucosal administered antigen that actually crossed the epithelial barrier[3,4], cannot be precisely determined but can only be estimated .Meanwhile mucosal tissues microenvironments are adapted to the presence of foreign antigens, such as microorganisms and their products. As a result, vaccines that consist of soluble macromolecules and protein subunit antigens, which may produce vigorous immune responses if injected into a sterile environment such as muscle, are often ignored when applied onto the mucosal surfaces[1,3,4,5,6]

The development of specific antibody- or T-cell-mediated immunologic responses and the induction of mucosal induced systemic immunologic hypo-responsiveness (oral or mucosal tolerance) depend on complex sets of immunologic events, including the nature of the antigenic stimulation of specialized lymphoid structures in the host, antigen-induced activation of different populations of regulatory T cells (Th1 versus Th2), and the expression of proinflammatory (IL-1, IL12 and immune-regulatory cytokines IL-10.[5,16].

So present study aim to evaluate the immune responses of S. typhi antigen both in mucosal and intramuscular primed lapin model.

2. Main Body

2.1. S. Typhi "O" Vaccine

Local S. typhi isolate characterized by API20 was obtained from an enteric fever cases[7]. S. tyhpi"O" antigen was heat killed bacteria [8].

2.2. Rabbits

Fourteen male New Zeeland white rabbits weighing 1.5 -2 kg were kept and housed individually in wire-rod floored and stainless steel cages each measuring 48x 61x46 cm with collection pan beneath each cage. Food and water were given ad libitum. They were grouped into two groups.

2.3. S. typhi Immunizations

Group I received two oral doses of S. typhi"O" bacterin (10 IU) one week a part.

Group II received two Intramuscular doses, one week a part. Rabbits of groups I and II were left one week then  bled.

2.4. Blood Sampling

Blood were collected through cardiac puncture method using sterile disposable syringes, from each animal in each group. Each sample without anti- coagulant for separation of sera to study agglutination[10], ELIZA IgM and IgG and cytokines, cytokine IL-1 alpha, IL-10 and IL-12 determination was performed as in manufacture instructions.

2.5. Antibody Score

The anti-Salmonella typhi antibody titer was scored as the reciprocal of the highest dilution that gave frank positive agglutination results[10] .S. typhi specific IgM and IgG were scored as an index mean values.

2.6. Cytokine Score

The cytokine responses were estimated as an immuno-enzyme color reactions in terms of picograms per milliliters.

2.7. Biometric Analysis

Biometery and graphs were done using PRISIM software.

3. Results and Discussion

Salmonella typhi specific agglutinin of intramuscular administrated antigen 560 ± 51.64in the S. typhi priming rabbite were of higher mean values than that of mucosallyadmintratedS. typhi antigen 40± 0 mean values.

Table 1. Salmonella specific serum agglutination titers and anti S. typhiIgG and IgM ELISA antibody index values.

Test rabbits Oral Rout Intramuscular Rout
agglutination IgG IgM agglutination IgG IgM
1 40 0.116 0.042 640 0.229 0.595
2 40 0.017 0.164 640 0.971 0.750
3 40 0.012 0.113 360 0.980 0.755
4 40 0.011 0.052 640 0.600 0.519
5 40 0.013 0.084 360 0.560 0.516
6 40 0.020 0.067 640 0.960 0.601
7 40 0.010 0.050 640 0.570 0.701
Mean 40 0.028 0.08 544.4 0.668 0.627

S. typhi specific IgM and IgG: The mean index value of IgM and IgG indicate specific for S. typhi in mucosal primed rabbits were(0.028± 0.014) lower than those intramuscular primed rabbits (0.6957± 0.10).

The Cytokine concentration level of S. typhi "O" primed rabbits for the cytokine IL-1 αand IL-10 were lower in mucosal than in intramuscular and they were equated for IL-12.(23.607 and 23.17) respectively p=0.01

The oral mucosal immune tolerance were screened by agglutination, IgG, IgM and IL-10. (Table-1, Figure 1-3).

Significantly different (P < 0.05)

Fig. 1. Agglutination titer for both oral and intramuscular(IM) administrated antigen.

(A) (B)

Significantly different (P < 0.05)

Fig. 2. Comparison IgG (A) and Igm (B) ELIZA antibody index values  in both Oral and Intramuscular rout.

 

Table 2. Cytokine profile of S. typhi primed rabbits .

Test Rabbits Cytokine profile pg/ml
IL-1 alpha IL-12 IL-10
Oral IM Oral IM Oral IM
1 125.98 153.549 1.2 23.45 2.1 24.0
2 125.08 437.667 1.4 5.7 2.5 24.3
3 98.42 102.36 10.2 27.005 1.8 22.3
4 55.11 200.14 10.8 42.788 1.3 26.2
5 141.73 211.11 10.8 14.03 1.3 26.2
6 86.61 201.20 67.58 25.8 1.5 26.2
7 70.01 212.84 50.43 27.2 1.53 27.4
Mean 100.4± 12.09 217.089± 39.78 23.607 23.82 1.719± 0.16 25.23± 0.6636
Control 15.3 7.32 4.450

 

Table 3. Oral Systemic Tolerance in S. typhi primed rabbits.

Rout Agglutinin* IgG* IgM* IL-1 α* IL-12* IL-10*
Oral 40 0.028 0.08 93.277 23.607 1.846
Intramuscular 542 0.668 0.62 217.089 23.17 24.48
Negative Control 80 0.017 0.073 15.3 7.32 4.4509

*mean values of the immune function tests. IgM, IgG in index values, cytokines in pg/ml.

A

B

C

Significantly different (P < 0.05)

Fig. 3. Cytokines profile of  IL-1(A); IL-10 (B) and  IL-12 (C) Elisa  in both Oral and Intramascular rout.

The results presented in table 1 and figure 1-3 were showing an endeno for mucosal immune tolerance induction through oral priming immunization program.Such finding may provide an endewe that mucosal exposure to environmental macromolecules, infectious agents and dietary antigens can result in the immunological state of development of systemic hypo- responsiveness toward the inducing antigen [11].Low IL-12 apparently can not be of use as indicator to the development of oral mucosal immune tolerance, other observation improved that systemic administration of Abs to IL-12 (anti-IL-12) simultaneous with Ag feeding modestly enhanced the degree of tolerance in the peripheral lymphoid tissues, as shown by increased suppression of proliferative responses after in vitro re-stimulation, IL-12 negatively regulates two of the main mechanisms of oral tolerance, TGF-beta production and clonal deletion via apoptosis. in addition, they suggest that the combination of oral Ag feeding and systemic anti-IL-12 administration may be of benefit in the treatment of autoimmune diseases[12].

Result show high concentration of IL-1 alpha in both oral and intramuscular vaccination however it was higher in intramuscular rout than in oral rout, A number of observations support the hypothesis that the production and release of L-1alpha were as effective as for the induction of Ag-specific serum IgG, secretory IgG and IgA, systemic delayed-type hypersensitivity, and lymphocyte proliferative[13].

Th2 cytokine IL-10 was higher in intramuscular vaccinated animal and combined with high antibody concentration. Th2 cytokines IL-10 was higher in intramuscular rout than in mucosal rout and to be significant help in antibody production [14].IL-10 was considered important in induction oral tolerance[14,15].

Briefly, factors which favor the Th1 type of response (IFN-γ, IL-12, and intact cholera toxin abrogate mucosal tolerance, while factors which favor Th2 (IL-4 and IL-10) or Th3 (TGF-β) response enhance the development and persistence of mucosal tolerance [16,11].

It has been proposes that the role of mucosal tolerance is to provide immunologic homostasis in the gastrointestinal tract [17].

Mild rate of IgM isotype switching to IgG were noted in both of the immunization routes [18].

Animal models for immune tolerance are of primary important in biomedical researches. They are either those of neonates or that of mature conventional and / or transgenic [19]. Like murine model for lung transplantation [20], and human CD3 trasngenic mice [21]. The present lapin model of oral mucosal tolerance, mucosal application of S. typhi bacterin induce low specific agglutination, specific IgM, Specific IgG as well as a mild rate of class switching from IgM to IgG. The interleukine 1 alpha, IL-10 but not IL-12 were proved to be of use in evaluation of immune tolerance state in this developed model.Such developed model may has potential bearing for use for therapeutic trends in hypersensitivity, autoimmunity as well as allograft sustainment [22].


References

  1. Kaufmann, H, E,S; Rouse, B, T, Sacks, D.L. 2011. The Immune Response to Infection. ASM, USA. pp:105.
  2. Neutra M R, Kraenebahl J – P,1996,Antigen uptake by M cell for effective mucosal response,In Kiyono H,Ogra PL, McGee J R,eds, Mucosal Vaccines,Academic Press,London,3-14.
  3. Oleszewska W,Openshaw PJM ,2004,Mucosal VaccinesIn Kauffmann ed, Novel  Vaccine Strategies,Wiley,VCH,Verlag,GmbH&Co.,KGaA,Germany,343-359.
  4. Staats H F, McGee JR1996 ,Principles of Mucosal Vaccination.In, Kiyono H,Ogra P L, McGee,J R,eds,Mucosal Vaccines,Academic Press,London, 15- 33.
  5. Ogra P L ,1996,Mucosal Immunoprophlaxis:An introductory overview,In,Kiyono H,Ogra P L, McGee J R, eds,Mucosal Vaccines,Academic Press,London,3-14.
  6. Ogra P L, Faden Hand Welliver R C.2001. Vaccination Strategies for Mucosal Immune Responses. ClinMicrobiol Rev. 2001 Apr; 14(2): 430–445.
  7. Marth T, Strober W, Kelsall BL. 1996.High dose oral tolerance in ovalbumin TCR-transgenic mice: systemic neutralization of IL-12 augments TGF-beta secretion and T cell apoptosis. J Immunol. 15;157(6):2348-57.
  8. Willey J, Sherwood L, Woolverton C. 2008. Microbiology 7th ed. Prescott Harley &Kleins McGraw-Hill.
  9. Svanborg E C, Kulhavy R, Marlid S, Prince S JandMestecky J.1985. Urinary immunoglobulins in healthy individuals and children with acute pyelonephritis.Scand .J. Immunol.,305-313.
  10. Steven C D. 2010. Clinical Immunology and Serology: A Laboratory Perspective,3edFA Davis Company, Philadelphia.
  11. Marie-Christiane M, Valerie G R. 2001. Influence of Resident Intestinal Micro oral on the Development and Functions of the Gut-Associated Lymphoid Tissue. Microbial Ecology in Health and Disease. 13: 65–86.
  12. Herman F. Staats and Francis A. Ennis, Jr. 1999. IL-1 Is an Effective Adjuvant for Mucosal and Systemic Immune Responses When Coadministered with Protein Immunogens1, Herman F. Staats2 and Francis A. Ennis, Jr. The Journal of Immunology. 162: 6141–6147.
  13. Weiner HL. 2001. Oral tolerance: immune mechanisms and the generation of Th3-type TGF-beta-secreting regulatory cells. Microbes Infect. 3(11):947-54.
  14. Jiri M, Zina M, Charles O E. 2005. Immune response versus mucosal tolerance to mucosally administered antigens. J. Vaccine 23:1800–1803.
  15. -Barone K S, Tolarova D D, Ormsby I, Doetschman T, Michael J G. 1998. Induction of oral tolerance in TGF-β1 null mice. J Immunol. 161:154–160.
  16. Mowat A M, Weiner H L. Oral tolerance: physiological basis and clinical applications.1999. In: Ogra P L, Mestecky J, Lamm M E, Strober W, Bienenstock J, McGhee J R, editors. Mucosal immunology. 2nd ed. New York, N.Y: Academic Press;pp. 587–618.
  17. Mason KL, Huffnagle GB, Noverr MC, Kao JY. 2008. Overview of gut immunology. AdvExp Med Biol. 2008; 635:1-14. doi: 10.1007/978-0-387-09550-9_1.
  18. Jasvir S J, Mark J P ,Suman G, Laura K. Phillip W. Marry E B, and Steven D L, Lucill L. 2012. Salivary glands act as mucosal inductive sites via the formation of ectopic germinal centers after site-restricted MCMV infection. J.FASEB, 25(5): 1680-1696.
  19. Weigle W O, 1998, Immune Tolerance Model, In.Delves P J and Roitt I M ed. Encyclopedia of Immunology 2d ed , Vol.4, Academic Press, New York, 2359-2361.
  20. Jiang X, Nicolls M R, 2014, Working towards immune tolerance in lung transplantation, J. Clin. Invest., 124(3)967-970.
  21. Kubn C, You S, Valette F, Endert P V, Bach J-F, Waldmann H, Chatenoud L. 2011, Human CD3 transgenic mice: Preclinical testing of antibodies promoting immunological tolerance, Translat. Med, 3(68):678-78.
  22. ShnawaIMS. 2015. Oral mucosal immune tolerance versus oral immune silenceing:Minireview, Am. J. Biomed. Lif. Sci. 3(4-1)7-9.

Article Tools
  Abstract
  PDF(206K)
Follow on us
ADDRESS
Science Publishing Group
548 FASHION AVENUE
NEW YORK, NY 10018
U.S.A.
Tel: (001)347-688-8931