Polymorphisms of the Toll-Like Receptor-2 Gene in Patients with Leprosy and Their Healthy Contacts

Leprosy is an immunopathology caused by M. leprae; its evolution depends on immunological and genetic aspects of the host. The objective was verifying the relationship between SNPs 2029 and 2258 of the TLR-2 gene and leprosy. Blood samples from 127 individuals were analyzed: 45 patients, being 34 multibacillary (MB) and 11 paucibacillary (PB) and 82 contacts, in the municipal-ities of the State of Pará-Brazil. SNPs 2029 and 2258 of the TLR-2 gene were genotyped by sequencing on the ABI 3130 Genetic Analyzer (Applied Biosys-tems), analyzed using Fisher’s exact test. Distribution of SNP 2029 genotypes: all MB individuals presented the C/C genotype and the mutant (C/T) genotype was observed in contacts and PB. Alleles: all MB individuals presented only C allele and the mutant allele (T) was observed in contacts and PB. SNP 2258 genotypes: 79 contacts had G/G genotype and only 3 had G/A genotype, the MB group had only G/G genotype and the PB group was predominant G/G, with only 1 G/A genotype. Alleles: all MB individuals had allele G and the mutant allele (A) was observed in contacts and PB. The association between the SNPs and the susceptibility or protection to leprosy was not observed.


Introduction
Leprosy is an immunopathology caused by Mycobacterium leprae and the evolution of the infection depends on the host's immunological and genetic factors, being the North region considered the area with the highest leprosy endemicity in Brazil [1] [2].
Its tuberculoid (HT) (paucibacillary) form corresponds to high resistance to infection by M. leprae, being related to the Th1 cellular immune response. At the other pole, it is the form of high susceptibility, lepromatous leprosy (HV) (multibacillary), characterized by the deficiency of Th1 cellular immune response, consequently, excessive bacillary multiplication and spread of infection. Among these polar forms are the dimorphic forms of the disease. In HV, high concentrations of specific M. leprae antibodies are found in serum, such as anti-PGL1 (phenolic glycolipid-1), associated with exacerbation of the Th2 response [3] [4] [5].
The innate immune response is the first line of defense against M. leprae, being a crucial step for the development of the response against the bacillus, since it has essential effector components in combating the pathogen, and is able to target adaptive immunity. Several cells of the immune system are activated through their cell receptors to generate an antigenic response, such as Natural Killer cells, lymphocytes, among others. Among the receptors expressed by Natural Killer cells, the Toll-Like receptors (TLR) on the surface and cellular cytoplasm stand out in the innate immune response [6] [7]. Each member of the TLR family is activated by specific antigens that lead to different transcriptional activation profiles, initiating an appropriate immune response to the pathogen. These receptors recognize lipoproteins present in the bacillus and promote the differentiation of monocytes into macrophages and CD1b + dendritic cells, which in turn activate lymphocytes that release cytokines such as TNF-α and IL-12, promoting antimicrobial activity. Of all mammalian TLRs, TLR2 is the one that detects the broadest repertoire of molecular patterns in a wide variety of pathogens, including mycobacteria, which makes it of particular clinical importance [8] [9]. Because M. leprae, in the host, initiates cell signaling by activating the TLR1/TLR2 heterodimer, changes in these genes may be able to confer susceptibility to leprosy [8]. Thus, a study involving the detection of SNPs 2029 (rs121917864; exchange of cytokine to thymine) and 2258 (rs137853176; exchange of guanine to adenine) in the TLR2 gene in leprosy patients and their healthy contacts, relating to the immune response may elucidate important aspects susceptibility of individuals to leprosy.
Thus, this study aimed to verify the relationship between SNPs 2029 and 2258 of the TLR-2 gene and leprosy, describing and comparing the genotypes and alleles in leprosy cases and their healthy contacts.

Materials and Methods
The study included individuals from the municipality of Redenção and Altamira,

Results
In this study, the genotypes of 127 individuals were typified, being 82 individuals household contacts of patients, 34 MB and 11 PB. Of the 127 individuals analyzed, 78 were female and 49 male, with most of the contacts being female (64.5%), the majority of MB male (56%) and almost all PB female gender (91%) ( Table 1).
Regarding the age group, most contacts and individuals in the PB group were 32 to 46 years old and most individuals in the MB group were older than 46 years (39%, 54.5% and 42% and respectively) ( Table 2).
As for the distribution of the SNP 2029 genotypes of the TLR2 gene between the groups, it was observed that all MB individuals had the C/C genotype and the mutant genotype, C/T, was observed only in contacts and paucibacillaries (N DOI: 10.4236/oji.2020.103004 40 Open Journal of Immunology = 5 and 1, respectively; Table 3).
Regarding the distribution of the frequency of alleles for SNP 2029 between the groups, it was observed that all MB individuals presented only C allele and the mutant (T) allele was observed only in contacts and paucibacillaries (3%, 4.5%, respectively) ( Table 4).

Discussion
Despite advances in research, diagnosis and the establishment of a free and effective therapy, leprosy is still endemic in Brazil and other developing countries.
There have been many efforts by public agencies to eradicate the infection; however, in Brazil the disease still has active foci of transmission [10].
In recent years, several researches have been carried out in the field of molecular biology in order to ascertain the immunogenetic profile of the host against infections caused by mycobacteria, mainly due to the particularities regarding genes related to the cellular immune response Th1/Th2, in order to identify genetic components that may provide the opportunity for the infection to install in the host organism. Today, some sets of genes have been linked to leprosy susceptibility and resistance [11].
The immune response to leprosy depends on a cascade of factors ranging from the recognition of the pathogen by specific receptors that trigger the syn- In a study conducted with a Korean population of 45 HV patients, 41 HT and 45 controls, the mutation was identified only in HV patients, which led the authors to suggest the association of the T allele with the severe form of the disease [21] [22]. Contrary results were observed in the present study, since the T allele was not observed in any of the 34 HV patients, being quite rare in the population of this study, found only in 6 individuals with heterozygous genotype (C/T), being in 1 HT and in 5 healthy contacts. Thus, in this study, we observed a greater similarity between the PB and contact groups, in which the mutation was very rare and could be protective against leprosy and or its aggravated form.
Despite what was shown in the Korean population by Kang et al. [21] and observed in the present study, Malhotra et al. [22] did not identify polymorphism at position 2029 in an Indian population and Mikita et al. [23] did not identify in Japanese leprosy patients. However, these different results can be explained by the different genetic origins among different populations.
Pioneering study by Lorenz et al. [24] reported a new polymorphism in the  [25] demonstrated that the A allele was considered rare and/or absent in these populations.
In a study carried out with the Amazonian population, by Naveca [26], for a possible association with susceptibility to TB, the A allele of SNP 2258, was absent in the individuals analyzed and not associated with the disease. A study by Sanchez et al. [16] in a population in Colombia also demonstrated the A allele as rare in patients and controls, (0.64% and 1.33%, respectively), and thus also not relevant to the risk of TB in this population involved.
However, Ogus et al. [27] observed the A allele in 17.9% and 7.7% of patients and controls, respectively. When the reasons for the three genotypes were compared between the two groups, the A/A genotype proved to be more significantly associated with TB. The risk of developing TB was increased by 6.04 and 1.60 times for patients with genotypes A/A and G/A, respectively. Therefore, these data suggest that the substitution of arginine for glutamine at position 753 of the TLR2 gene influences the risk of developing tuberculosis.
In the present study, during an analysis of the distribution of the SNP 2258 genotypes of the TLR2 gene, the predominance among the population of the G/G genotype (96.4%) was detected, with allele A being found in one of the PB and three contacts and not found in MB, ratifying what was found in studies carried out on other populations and contributing information that the A allele is rare. Thus, in this study, we observed a greater similarity between the PB and Open Journal of Immunology contact groups, in which the mutation was very rare and could be protective against leprosy or its aggravated form.
In addition to the similarity observed between the PB and contacts groups in relation to the SNPs studied (although without statistical significance), a similarity was also observed in relation to the age group and sex (statistically significant), as these two groups are predominantly female with age group from 32 to 46 years old, while MB is the majority male with age group above 46 years old.
These data corroborate with other studies carried out by Bakker et al. [28] and Lima et al. [29].

Conclusion
To date, the results of this research do not indicate associations of SNPs 2029 and 2258 of the TLR2 gene and protection or susceptibility to leprosy, demonstrating that the sequences covering these regions are well conserved in the study population. Thus, due to the low frequency in the incidence of the SNPs studied in the investigated population, it is necessary to intensify the studies, in addition to investigating other regions of the genome that aim to clarify the involvement of TLR and the immune response triggered in the face of host-pathogen contact.

Ethical Clearance
This study was approved by the Ethics and Research Committee of the Instituto Evandro Chagas with the report number: 2.364.234.