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  IN THIS Article
 ::  Abstract
 ::  Introduction
 ::  The future
 ::  References

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REVIEW ARTICLE
Year : 1991  |  Volume : 37  |  Issue : 4  |  Page : 198-204

Anti-leprosy vaccines: current status and future prospects.


Cancer Research Institute (Tata Memorial Centre), Parel, Bombay, Maharashtra.

Correspondence Address:
Cancer Research Institute (Tata Memorial Centre), Parel, Bombay, Maharashtra.


  ::  Abstract

Different types of leprosy vaccines are currently used in field trials in India. The rationale behind their use, the parameters for determining their efficacy, their merits and demerits are discussed and the future prospects are highlighted.

How to cite this article:
Kartikeyan S, Chaturvedi R M, Deo M G. Anti-leprosy vaccines: current status and future prospects. J Postgrad Med 1991;37:198-204


How to cite this URL:
Kartikeyan S, Chaturvedi R M, Deo M G. Anti-leprosy vaccines: current status and future prospects. J Postgrad Med [serial online] 1991 [cited 2014 Nov 28];37:198-204. Available from: http://www.jpgmonline.com/text.asp?1991/37/4/198/759




  ::   Introduction Top

The word 'vaccine' is derived from the French 'la vacche' meaning the cow, a reference to the cowpox extract used by Jenner in 1812 to prevent smallpox in humans. Pasteur introduced the concept of attenuated vaccines. Vaccines act by enhancing host immunity and are, perhaps, the most effective means of controlling infectious diseases. The global eradication of smallpox could be achieved mainly because of the availability of a cheap and effective vaccine.
Generally, vaccines are prepared by using the killed or attenuated organisms that have lost their virulence but have retained their ‘protective’ antigens. A second option is to use a live attenuated or killed non-pathogenic organism that antigenically cross-reacts with the pathogen. A third approach would be to use only the immunogenic 'subunit(s)' of the organism. All the three approaches have been used in the preparation of a 'candidate' anti-leprosy vaccine[6],[9],[13],[35] [Table - 1].
In India, the second option of using antigenically related cultivable organisms is being actively pursued[5],[12],[13] [Table - 2].
A vaccine containing ICRC bacilli (which are cultivable leprosy derived mycobacteria probably belonging to M. avium intracellulare complex) was prepared in 1979 at the Cancer Research Institute, Mumbai[12]. Studies, both on humans and animals, show that the ICRC bacilli exhibit antigenic cross-reactivity with M.leprae with reference to both B and T cell antigens[8],[19],[20],[27]. The capacity of a large number of T4 + clones, developed from a patient of tuberculoid leprosy, have been tested in response to M.leprae soluble protein[17]. The reaction of several clones with ICRC bacilli suggests a close relationship with M.leprae with reference to T cell antigens. Studies also show that the antigens of the ICRC bacilli are also more accessible, making the organism a stronger immunogen.
One of the first vaccines to be used against leprosy was BCG. BCG was found effective against the growth of M.leprae in foot-pads of mice[30]. However, trials with the BCG vaccine on human beings at four major places showed varied results[18]. In Uganda, a protection of 80% was observed, while that in Papua New Guinea was 46%. Trials in South India showed 28% protection and in the Burmese trial, it was 20%. Thus, it has been concluded that the protective effect of BCG has generally been modest, except in Uganda. By itself, BCG vaccination is no more considered to be a modality for immunoprophylaxis of leprosy.
Although M.leprae is yet to be cultivated, it grows profusely in armadillos[25]. Convit et al showed that the immunogenicity of M.leprae (which is a weak immunogen) is enhanced by the addition of BCG[10] and subsequently established the concept of a mixed vaccine containing a mixture of heat-killed armadillo-derived M.leprae (M.leprae-A') + BCG. The mixed vaccine induces immunological changes both in leprosy patients and in health persons but either organism given alone is ineffective. No information is available on the stability of the immune conversion and on antigenic variation, if any, between M.leprae obtained from different armadillos. This mixed vaccine is currently undergoing trials in Venezuela and Malawi.
A vaccine prepared from Mycobacterium welchii (M.W.) has been shown to induce lepromin conversion in BL/LL patients[5]. M.W.,a rapid growing mycobacterium is said to be a cultivable saphrophytic soil bacillus[14]. The vaccine has been used in patients with multibacilliary leprosy and the results are similar to those obtained with the ICRC vaccine[12],[36]. But this should not be surprising because ICRC and M. W. are similar with reference to cell antigens[20],[27].
Scientists at the Central Drug Research Institute Lucknow have shown CMI response in mice M and in langur and rhesus monkeys[14] using a vaccine prepared from M.habana, a photochromogenic atypical mycobacterium.
Stanford et al have demonstrated lepromin conversion in humans using a mixed vaccine containing BCG and killed M. vaccae[32].
According to Mahadevan et al, the lipid component of cell wall of M.leprae prevents the recognition of bacilli by macrophages and is thus responsible for anergy seen in LL patients. However, patients with TT leprosy exhibit CMI response due to high levels of serum lipase, which removes the lipids of the cell wall. Delipidified cell component (DCC) of M.leprae have been shown to activate macrophages and kill M.leprae in vitro[29]. Its safety and toxicity studies are in progress.
Parameters For Determining Vaccine Efficacy:
The ultimate of any vaccine is determined by its ability to lower the incidence of the disease. Leprosy is a disease with a long incubation period and therefore, such studies would take many years to complete. Before such long term large scale field studies are initiated, it would be essential to show, both in experimental and clinical studies, that the 'candidate' vaccine is capable of effecting immunological changes that portray 'protective' immunitly. In the present state of our knowledge, cell mediated immunity (CMI) is the dominant host defence against M.leprae and circulating anti-M.leprae antibodies have little role.
Much of the vaccine development in leprosy is based on response to skin tests with soluble and integral (Mitsuda) antigens of M.leprae[16]. Though the relationship between skin response and protective immunity is yet to be established, among the available tests, the Mitsuda test correlates best with the capacity of the host to handle M.leprae, while the lymphocyte transformation test (LTT) is not considered a good index of protective immunity[3]. On the other hand, the Mitsuda test is also a good indicator of host susceptibility in armadillos[22] and monkeys[34] - the two species that develop disseminated M.leprae disease. Mitsuda negative individuals living in endemic areas run a high risk of contracting multibacillary forms of leprosy[15] and in untreated patients, the Mitsuda test is inversely related to the tissue bacillary load[28].
Leprosy is a spectral disease in which the clinical and pathological features reflect the CMI of the host[28]. There is a progressive improvement in CMI and a reduction in the tissue bacillary load from the lepromatous (LL) to the tuberculoid (TT) end of the spectrum. 'Upgrading' in the spectrum, therefore, indicates improved CMI. A candidate vaccine should be able to induce 'upgrading' in the anergic LL patients and bring about lepromin conversion in both the patients and lepromin negative healthy sibjects. Ideally, a candidate vaccine should also show protection in animal models. However, there are no suitable animal models for leprosy. From the data presented at the Pre- congress Workshop on 'Leprosy Vaccine Trials' held under the auspices of the XIII International Leprosy Congress at The Hague in September 1988, it was clear that the studies on mouse foot- pads (the most widely used laboratory model) have given variable results in different laboratories with reference to all candidate vaccines (Sengupta, U., Personal communication).
From The Laboratory To Large Scale Field Studies:
Studies with the ICRC vaccine since 1979 show that a single dose of the vaccine brings about persistent immune conversion in 53% of LL patients on chemotherapy, associated in some patients with 'upgrading' of tissue reaction and accelerated clearance of bacilli from the tissues of the patients[12],[13]. About 10% of the patients had post-vaccination reversal reactions[1] and about a third of the patients with a high bacillary index developed ENL 10-15 days after vaccination[12]. Despite the upgrading, no fresh nerve lesions were observed in the vaccinated patients [12],[13]. Similar findings have been reported by Convit et al, in their studies[9],[10]. The ICRC vaccine induces immune conversion in 95% of lepromin-negative healthy sibjects in endemic areas[4] and the conversion was found to be stable for 5 years. These clinical observations are supported by the results of studies carried out in our monkey mode[7].
Until 1984, the vaccine had been tried only on LL patients and lepromin-negative healthy persons. However, in large scale field studies, the vaccine would have to be administered to volunteers without subjecting them to a pre-vaccination lepromin test. Thus, the target population would include both lepromin positive and negative individuals, which would be a sub-set of the general population. Hypersensitivity to M.leprae antigens, to which the residents of an endemic area are exposed continuously, has been implicated in the pathogenesis of nerve damage in leprosy[21],[33]. Lepromin positive vaccines could be at a major risk of developing neural lesions since they already possess a strong CMI to the antigens of M.leprae. But such fears have been allayed by the results of the pilot study, which was conducted under field conditions, about 100 kin from Mumbai. No untoward effects have been observed during the last 4 years in both lepromin positive and negative healthy household contacts (HHC) of multibacillary leprosy patients, who were given the ICRC vaccine[4]. The vaccine is safe and well tolerated and its acceptability is high since it is given as a single dose. This vaccine has no effects on antibody levels[4]. Circulating anti-M.leprae antibodies have little role in host defence against leprosy, but these have been implicated in certain Hyperseitsitivity reactions[12],[33]. Antibodies could also form immune complexes that might suppress CMI. As the ICRC vaccine is developed from a cultivable organism, it will be cheap and there will be no chance of contamination with animal products. This vaccine also induces stable immunity unlike vaccines that contain armadillo-derived M. leprae.
The large scale field studies of the ICRC vaccine were launched in February 1987 in south-eastern part of Maharashtra [Figure:1]. The prevalence rates for leprosy in this area vary between 8 to 10 per thousand. The studies are randomised, controlled and involve HHC of leprosy patients. A comparative evaluation of the two mycobacterial vaccines (ICRC and BCG) will be made by measuring the incidence of all forms of leprosy in the vaccines. The vaccines are of both sexes between 1 and 65 years of age. Pregnant women, and persons with chronic debilitating diseases, severe malnutrition history of allergic reactions, epilepsy and tuberculosis are excluded from the studies. On the basis of the list of leprosy patients provided by the Leprosy Control Units of the Government of Maharashtra, the patients are visited on a house-to-house basis and only house hold contacts (HHC) of patients with signs of active disease participate in the programme. Simultaneous to the clinical examination, the vaccines are given randomly to the eligible HHCs, intradermally in the right deltoid region. Both vaccines produce a comparable local reaction consisting of delayed inflammation and ulceration that heals in 4-6 weeks. No systemic reaction in usually seen.
The sample size for the two-arm study with a five-year follow-up would be 31,000. The intake has been completed. The vaccines would be followed-up for 10 years.

  ::   The future Top

The science of vaccinology has come a long way from the 'first generation' vaccines that contain the whole organism [Table - 1]. The whole organism, attenuated or killed, may contain some antigen(s) that may be immunosuppressive, making the vaccine less effective. Moreover, such a vaccine may produce undesirable side effects. These problems could be overcome by using only the 'protective' immunogenic 'sub-unit'. It is now recognised that the immunogenicity of a protein molecule resides in segments of its small peptides[22]. A vaccine containing only the peptide possessing the specific immunogenic epitopes will be 'purer' and such peptides could be synthesized chemically or biosynthesized using recombinant DNA technology.
So far, M.leprae has resisted attempts at cultivation and this could be limiting factor in preparation of large quantities of a 'sub-unit' vaccine. Using recombinant technology, the entire genome of M.leprae has been cloned[35]. Recombinant DNA clones containing gene coding for 5 immunogenic proteins have been isolated using monoclonals. If scientists succeed in identifying the 'protective' antigen(s) from amongst these proteins, the non-cultivability of M.leprae would no longer be a constraint since the clones making 'protective' antigen(s) could be a constant source of supply for the preparation of a vaccine.
Scientists at the Cancer Research Institute, Mumbai, have adopted the alternative strategy of fractionation of the sonicate of ICRC bacilli to identify its immunogenic 'subunit(s)[6],[8]. On high Performance Liquid Chromatography using gel permeation columns, the sonicate yields a very high molecular weight fraction (approx. 1 million daltons) named PP-1, which is the dominant T-cell immunogen of the ICRC bacilli[8]. A similar fraction has been isolated from the sonicate of M.leprae. The PP-I fractions of the two organisms exhibit antigenic cross- reactivity. PP-I is a glycoprotein and is probably a component of cell walls. Recently, a very high molecular weight cell wall core (CWC) fraction has been isolated from M.leprae. CWC is also a strong T-cell immunogen[23]. A vaccine containing PP-I of ICRC bacilli induces lepromin conversion in lepromatous patients and their lepromin-negative HHC[2],[6]. Being a glycoprotein, PP-I contains all the components essential for vaccine. Its proteins could act as antigens or carriers for carbohydrates or lipids which could by themselves act as antigens. In addition, the lipids would also provide a built-in adjuvant. This vaccine containing PP-I of ICRC bacilli is currently undergoing Phase-I and II clinical studies in India.
Leprosy and tuberculosis are the two dominant mycobacterial diseases that are major health problems in the Third World. Mycobactetium avium intracellulare group of organisms have acquired a special significance in developed nations too, because of their frequent isolation from AIDS patients[24].
Since the ICRC bacillus belongs to the M.leprae intracellulare (MAI) complex, the vaccine may also act against infections caused by these opportunistic microbes[11]. A mixed vaccine containing BCG and ICRC bacilli or their immunogenic 'sub-units' could be the future polyvalent mycobacterial vaccine that might offer protection against a wide spectrum of mycobacterial diseases. Such a polyvalent mycobacterial vaccine would reduce the number of vaccinations and thus would be of tremendous operational advantage to health authorities especially in the Third World.

  ::   References Top

1. Bhatki WS, Chulawala RG, Bapat CV, Deo MG, Reversal reaction in lepromatous patients induced by a vaccine containing killed ICRC bacilli a report of five cases. Int J Lepr 1983; 51:466-472.  Back to cited text no. 1    
2.Bhatki WS, Chulawala RG, Chaturvedi RM, Dixit GM, Deo MG. Lepromin conversion induced by a 'sub-unit' vaccine from ICRC bacilli. Ind J Med Res 1988; 87:545-554.  Back to cited text no. 2    
3.Bjune G, Barneston R St. C, Ridley DS Kronvall G. Lymphocyte transformation test in leprosy-correlation of the response with inflammation of lesions. Clin Exp Immunol 1976; 25:85-94.  Back to cited text no. 3    
4.Chaturvedi RM, Chirmule NB, Yellapurkar MV, Shaikh SU, Deo MG. Effects of ICRC anti-leprosy vaccine in healthy subjects. Int J Lepr 1987; 55:657-666.  Back to cited text no. 4    
5.Chaudhary S, Fotedar A, Talwar GP. Lepromin conversion in repeatedly lepromin negative BL/LL patients after immunization with autoclaved Mycobacterium W. Int J Lepr 1983; 51:159-168.  Back to cited text no. 5    
6.Chirmule NB, Chaturvedi RM, Deo MG. Immunogenic “sub-unit” of the ICRC antileprosy vaccine Int J Lepr 1988; 56:27-35.  Back to cited text no. 6    
7.Chirmule NB, Deo MG, Shirodkar MVN, Deshmukh R, Chanderkar NG. ICRC vaccine-induced changes in Mleprae-specific cell mediated immunity in Langur (Presbytis entellus) monkeys. Int J Lepr 1986; 54:57-62.  Back to cited text no. 7    
8.Chirmule NB, Mulherkar R, Deo MG. Antigenic profile of ICRC bacilli with special reference to isolation of immunogenic sub-unit. Int Arch Allergy Appl Immnu 1988; 86:19-27.  Back to cited text no. 8    
9.Convit J, Aranzazu N, Ulrich M, Zuniga M, de Aragon ME, Alvarado J, Reyes O, et al. Investigations related to the development of a leprosy vaccine. Int J Lepr 1983; 51:531-539.  Back to cited text no. 9    
10.Convit J, Uirich M, Aranzazu N. Vaccination in leprosy-observations and interpretations Int J Lepr 1980; 48:62-65.  Back to cited text no. 10    
11.Deo MG. Immunological approach for control of Mycobacterium avium-intracellulare infections in AIDS-an hypothesis. Int J Lepr 1988; 56:455-463.  Back to cited text no. 11    
12.Deo MG, Bapat CV, Bhalerao V, Chaturvedi RM, Bhatki WS, Chulawala RG. Antileprosy potentials of ICRC vaccine. A study in patients and healthy volunteers. Int J Lepr 1983; 51:540-549.  Back to cited text no. 12    
13.Deo MG, Bapat CV, Chulawala RG, Bhatki WS. Potential anti-leprosy vaccine from killed ICRC bacilli a clinicopathological study. Ind J Med Res 1981; 74:164-177.  Back to cited text no. 13    
14.Dharmendra: (ed) Leprosy: Volume 2. Samant and Company, Mumbai 1985.  Back to cited text no. 14    
15.Dharmendra KR, Chatterjee KR. Prognostic value of the lepromin test in contacts of leprosy cases. Int J Lepr 1956; 24:315-318.  Back to cited text no. 15    
16.Editorial. Vaccines against leprosy. Lancet i: 1987; 1183-1184.  Back to cited text no. 16    
17.Emmrich F, Kaufmann SHE. Human T-cell clones with reactivity to Mycobacteritan leprae as tools for the characterization of potential vaccines against leprosy. Infect Immunity 1983; 51:879-883.  Back to cited text no. 17    
18.Fine PEM. Leprosy: Epidemiology of a slow bacterium. Epidemiol Revs 1982; 4:161-188.  Back to cited text no. 18    
19.Gangal SG, Khanolkar SR. Delayed hypersensitivity in vitro to an acid fast mycobacterium cultivated from human lepromatous leprosy. Ind J Med Res 1974; 62:290-296.  Back to cited text no. 19    
20.Girdhar BK, Desikan KV. Results of skin tests with five different mycobacteria. Lepr India 1978; 59:555-559.  Back to cited text no. 20    
21.Godal T. Immunological aspects of leprosy: Present status. Prog Allergy 1978; 25:211-242.  Back to cited text no. 21    
22.Job C, Kirchheimer WF, Sanchez RM. Tissue response in lepromin, an index of susceptibility of the armadillo to M.leprae infection a preliminary report. Int J Lepr 1982; 50:177-182.  Back to cited text no. 22    
23.Kaplan JM, Hunter SW, McNeil M, Stewart C, Modlin RL, Rea TH, Convit J, Salgame P, Mehra V, Bloom BR, Brennan PJ, et al. Immunological significance of Mycobacterium leprae cell walls. Proc Natl Acad Sci USA: 1988; 5:1917-1921.  Back to cited text no. 23    
24.Kichn TE, Edwards FF, Brennan PJ, Tsang AY, Maio M, Gold JW, Whimbey E, Won B, McClatchy JK, Armstrong D. Infections caused by Mycobacterium avium complex in immunocompromised patients. J Clin Microbiology 1985; 21:168-173.  Back to cited text no. 24    
25.Kirchheimer WF, Storrs EE. Attempts to establish the armadillo (Dasypus novemcintus Linn) as a model for the study of leprosy. 1-Report of lepromatoid leprosy in an exptally infected armadillo. Int J Lepr 1972; 39:693-702.  Back to cited text no. 25    
26.Liew FY. New aspects of vaccine development. Clin Exp Immunol 1985; 62:225-241.  Back to cited text no. 26    
27.Mustafa AS, Talwar GP Five cultivable mycobacterial strains giving blast transformation leukocyte migration inhibition of leukocytes analogous to Mycobacteritun leprae. Lepr India 1978; 50:498-508.  Back to cited text no. 27    
28.Ridley DS, Jopling WH. Classification of leprosy according to immunity. A five group system. Int J Lepr 1966; 34:255-273.  Back to cited text no. 28    
29.Robinson P, Mahadevan PR. Immune modulation of deficient cells from leprosy patients leading to killing of M.leprae in vitro demonstration. Poster Presentation at XVI I.A.L. Conference, Trichur, November, 1989.  Back to cited text no. 29    
30.Shephard CC, Van Landingham R, Walker LL. Searches among mycobacterial cultures for anti-leprosy vaccines. Infect Immun 1980; 29:1034-1039.  Back to cited text no. 30    
31.Singh NB, Srivastava A, Gupta HP, Desikan KV. Immunological potential of a cultivable mycobacteria strain M.habana against leprosy bacillus in mouse foot pad. Indi J Leprosy 1985; 57:273-277.  Back to cited text no. 31    
32.Stanford JL. A pilot study of 3 potential vaccines for leprosy in Mumbai school children. Proceedings of XIII International Leprosy Congress at the Hague 1988, pp 241 (Abstract).  Back to cited text no. 32    
33.Waters MFR, Turk JL, Wemambu SNC. Mechanisms of reaction in leprosy. Int J Lepr 1971; 39:417-428. .  Back to cited text no. 33    
34.Wolf RH, Gormus BL, Martin LN, Baskin GB, Walsh GP, Mevers WM, Binford CH, et al. Experimental leprosy in three species of monkeys. Science 1985; 227:529-531.  Back to cited text no. 34    
35.Young RA, Mehra V, Sweetser D, Buchanan T, Clark-Curtiss J, Davis RW, Bloom BR, et al. Genes for the major protein antigens of the leprosy parsite Mycobacterium leprae. Nature 1985; 316:450-452.  Back to cited text no. 35    
36.Zaheer SA, Talwar GP, Walia R, Mukherjee R, Sharma AK, Kar HK, Mukherjee A, et al. Results of one year Phase- II/Phase III trials with a candidate anti-leprosy vaccine containing Mycobacterium W. Proceedings of XIII Int Lepr Congress 1988, pp 241 (abstract).   Back to cited text no. 36    

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