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HLA Association with Drug-Induced Adverse Reactions.

1. Introduction

Major histocompatibility complex (MHC) are a group of cell surface proteins that can bind to foreign molecules in order to be recognized by corresponding T cells followed by inducting immune systems. MHC is highly conserved and presents in all vertebrate species. In human, MHC is also known as human leukocyte antigen (HLA) complex, which consists more than 200 genes on chromosome 6 and can be categorized into three subgroups: class I, class II, and class III. Class I MHC, being recognized by CD8+ T cells, consists of three main genes, that is, HLA-A, HLA-B, and HLA-C. Class II MHC, being recognized by CD4+ T cells, consists of 6 main genes, that is, HLA-DPA1, HLA-DPB1, HLA-DQA1, HLADQB1, HLA-DRA, and HLA-DRB1.

HLA class I molecules are expressed in almost all the cells and are responsible for presenting peptides to immune cells. Generally, old proteins in the cells will be broken down consistently in order to synthesize new peptides. Some of these broken peptide pieces attach to the MHC molecules and are further recognized by immune cells as "self." In another situation, if a cell is infected by pathogens, pathogenic peptides attached to MHC molecules will be recognized as "nonself" and further trigger the downstream immune responses against the antigens [1]. HLA genes are found to be numerous and highly polymorphic in order to bind various kinds of peptides originated from self or foreign antigens. A total of more than 1500 alleles of HLA-B gene have been identified [2]. Variations in the HLA genes play an important role in determining the susceptibility to autoimmune disease and infections; they are also critical in the field of transplant surgery where the donors and the recipients must be HLA-compatible [3].

In rare cases, some drugs are capable of inducing immune responses through interactions with MHC molecules, known as adverse drug reactions (ADRs). ADRs are one of the most common causes of hospitalization and mortality in healthcare. The definition of an ADR has been changed from time to time. In the 1970s, the World Health Organization (WHO) has first defined that an ADR is "a response to a drug that is noxious and unintended and occurs at doses normally used in man for the prophylaxis, diagnosis or therapy of disease, or for modification of physiological function" [4]. However, in most cases, the ADRs might not result in effects as severe as harms or injuries like the word "noxious" addressed by WHO. Therefore, Edwards and Aronson [5] suggested to use an alternative definition; that is, an ADR is "an appreciably harmful or unpleasant reaction, resulting from an intervention related to the use of a medicinal product, which predicts hazard from future administration and warrants prevention or specific treatment, or alteration of the dosage regimen, or withdrawal of the product." It is also defined as "an undesirable effect, reasonably associated with the use of the drug that may occur as a part of the pharmacological action of a drug or may be unpredictable in its occurrence."

2. ADRs Associated with Immunological Reactions

Several studies showed that ADRs are a major public health problem worldwide, which account for about 6.5% of all hospitalizations in the United States, Canada, and the United Kingdom, and it also resulted in a mortality rate approximate to 0.13% [6-8]. ADRs could be categorized into 6 different types [5]. Among them, type B, also known as non-dose-related or bizarre, is unpredictable and results in a high mortality rate oftentimes. This type of ADRs is usually associated with immunological reactions involving different HLA alleles and resulted in skin injury, hepatic failure, or dramatically reduced numbers of white blood cells.

Skin injury includes various kinds of spectrum such as mild rash maculopapular exanthema (MPE), fixed drug eruption (FDE), acute generalized exanthematous pustulosis (AGEP), and life-threatening severe cutaneous adverse drug reactions (SCARs) including drug reactions with eosinophilia and systemic symptoms (DRESS), Stevens-Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN) [9]. Patients who developed MPE are usually observed with generalized, widespread mild skin rashes with red macular (not elevated) or papular (elevated) eruptions. FDE can be diagnosed by observing one or more local annular or oval erythematous patches without hyperpigmentation. The term "fixed" is considered as its recurrent lesion due to reexposure of the same culprit drug, and the lesions always occur at the same locations on the skin. AGEP is a rare, acute eruption characterized by the rapid development of many numerous pustules, which are nonfollicular sterile pustules, and is located in the epidermis. Fever, leukocytosis, and eosinophilia are usually present in AGEP patients.

SJS, SJS, and TEN overlap (SJS/TEN) and TEN are classified as the same disease spectrum with increasing severity and with extent of widespread epidermal detachment, known as SCARs [10]. All of them usually present with a variety of skin lesions, including patches, atypical targetoid macules, and erythematous or violaceous macules. In addition, SJS/TEN often has mucocutaneous involvement, which is the characteristic feature of SJS/TEN. In addition, the oral mucosa is more commonly involved than the ocular, genital, or anal mucosa. The degree of skin detachments of SJS, SJS/TEN, and TEN are defined as less than 10%, 10-30%, and 30% of body surface area, respectively. Full-thickness epidermal necrosis is a typical pathological feature of SJS/TEN. The clinical characteristics of DRESS are different from SJS/TEN. DRESS usually presents less or no skin detachment and no mucocutaneous involvement but with more internal organ involvement and hematological abnormalities such as typical eosinophilia, atypical lymphocytes, hepatitis, and high fever with frequent reactivation of human herpesvirus. Histopathological characters of DRESS are epidermal spongiosis, dyskeratosis, and interface vacuolization.

Other than skin injury, hepatic failure, such as drug-induced liver injury (DILI), is rare but life threatening. DILI is different from drug overdose toxicity in which the risk and severity of such kind of liver injury usually increases with the dose taken. DILI accounts for 7-15% of the cases of acute liver failure in Europe and the United States [11-13]. Up to 10% of DILI can progress to acute liver failure in the US and European studies, and the incidence is estimated to be 2.4 per 100,000 person-years (in a retrospective population-based study of 1.64 million UK subjects) [14] to 13.9 per 100,000 inhabitants (in a prospective analysis in France) [15].

Agranulocytosis, also known as agranulosis or granulopenia, is an acute condition involving a severe and dramatic decreasing of white blood cell counts, which is life threatening. It is recently reported to be induced by antithyroid drugs in rare situations and is associated with HLA alleles [16].

3. Hypothesis of Immune Response

Drugs or its reactive metabolites are considered as foreign antigens that bind to T cell receptors (TCR) and further activate immune response. Four hypotheses have been proposed to explain how the immune system is activated in a HLA molecule-dependent manner: (i) the "hapten/prohapten" theory, (ii) the "p-i" concept, (iii) the "altered peptide repertoire" model, and (iv) the "altered TCR repertoire" model [17, 18].

The "hapten/prohapten" theory proposes that a drug or its reactive metabolite may bind covalently to an endogenous peptide to form an antigenic hapten-carrier complex. In this model, the covalent bonds are established among the drug (or its metabolite), self-peptides, and HLA molecule. It then results in the induction of drug-specific immune responses.

The "pharmacological interaction with immune receptors (p-i)" concept postulates that a drug or its reactive metabolite may directly, reversibly, and noncovalently bind to the HLA and/or TCR without binding to the antigenic peptide. In this "p-i" model, the classic antigen-processing pathway in antigen-presenting cells may be bypassed.

The "altered peptide repertoire" model proposes that a drug could strongly bind to the self-peptide repertoire and alter the conformation of this peptide repertoire presented to HLA and TCR. In the "altered peptide repertoire" model, the drug may not directly bind to HLA.

Finally, the "altered TCR repertoire" model suggests that the drug (e.g., sulfamethoxazole) binds to the specific TCR and alters the conformation of TCR, which has the potential to bind a HLA-self peptide complex to elicit immune reaction. In the "altered TCR repertoire" model, the TCR serves as an initial drug interaction molecular. With the binding of an offending drug presented to the HLA molecule or TCR, the HLA-drug-TCR complex may trigger a series of activations of cell signaling and result in an expansion of cytotoxic T lymphocytes (CTL), cytotoxic protein secretions, and keratinocyte death in patients with SJS/TEN. A recent study has shown the importance of TCR in the pathogenic mechanism of SJS/TEN onset by clarifying the shared and restricted TCR use in carbamazepine-induced SJS/TEN patients [19]. Additionally, another interesting study demonstrated that the endogenous peptide-bound HLA-B* 15:02 molecule presents carbamazepine to TCR of CTL to initiate the immune reactions in carbamazepine-induced SJS/TEN [20].

4. Drugs and HLA Alleles

A couple of drugs have been proposed to induce HLA-associated ADRs (Table 1). In this section, we summarized some of the well-known drugs and the HLA alleles associated with ADRs induced by these drugs. For more detailed information, please see the list in Table 1.

4.1. Abacavir Hypersensitivity and HLA-B*57:01 (Skin). Abacavir is a nucleotide reverse transcriptase inhibitor used as part of adjuvant therapy in human immunodeficiency virus- (HIV-) infected patients. In 5-8% of treated patients, abacavir can cause hypersensitivity responses. More than 90% of the patients with hypersensitive syndrome start within 6 weeks of treatment and require immediate cessation of the medication. Re-exposure of the abacavir leads to rapid appearance of symptoms and higher chance to induce more severe symptoms [21]. Symptoms reported including fever, rash, malaise/fatigue, and gastrointestinal symptoms such as nausea, vomiting, and diarrhea. Respiratory symptoms occurred in 30% of cases including dyspnea, cough, and pharyngitis. In very rare cases, abacavir might result in more severe reaction such as SJS/TEN [22, 23].

In 2002, two publications first proposed that abacavir hypersensitivity was significantly associated with the presence of allele HLA-B* 57:01 in Australian and British cohorts [24, 25]. Saag et al. [26] further demonstrated that there is a higher chance of developing hypersensitivity in Caucasians than African-Americans who were treated with abacavir. Among those suffered from abacavir hypersensitivity, 44% of Caucasians and 100% of African-Americans showed positive of HLA-B*57:01 allele. Recently, HAL-B*57:01 was screened in other populations (summarized in Martin et al. [27]). In general, the frequency of HLA-B*57:01 allele is much higher in Caucasians than in other populations. In Taiwan, abacavir hypersensitivity is less frequent, as it occurs in approximately 0.3% of HIV-infected patients who undergo abacavir-containing combination antiretroviral therapy (a total of 320 patients studied). The possible reason might be the low frequency of the HLA-B* 5701 allele in Taiwanese population [28].

The mechanisms of abacavir hypersensitivity is better studied compared to other drug-induced ADRs. It is thought that short peptide fragments, derived from either the drug or its metabolites, form a peptide-HLA complex specifically with HLA-B* 57:01. This complex activates CD8+ T cells, which release inflammatory cytokines and start the hypersensitivity response. More recently, it has been shown that abacavir might occupy a space below the region of HLA that presents peptides, which leads to an altered peptide presentation and trigger an autoimmune reaction [29]. By using X-ray crystallography and structural analysis, Yerly et al. further proposed that the hypersensitivity reaction is due to both types of T cells that recognize self-peptide/HLA-B* 57:01 complexes and cross react with viral peptide/HLA-B* 57:01 complexes due to similarity in drug-specific T cell receptors contact residues [30].

As genetic screens for HLA-B* 57:01 could significantly reduce the incidence of abacavir hypersensitivity in Caucasians, the European Medicines Agency and US Food and Drug Administration (FDA) recommend prospective screening for HLA-B*57:01 for patients who are considered to undergo abacavir treatment [27, 31].

4.2. Carbamazepine and Oxcarbazepine Hypersensitivity and HLA-B* 15:02, HLA-B* 15:11, and HLA-A*31:01 (Skin). Carbamazepine is an important drug used in the treatment of epilepsy, trigeminal neuralgia, and bipolar disorder [32-34]. In 2004, Carbamazepine was first reported to be strongly associated with allele HLA-B* 15:02 by studying patients developed SJS/TEN in Taiwan (OR > 1000) [35]. This association was validated in different populations, including those in Thailand, Malaysia, Singapore, and India [36-38]. A large scale of prospective study including almost 5000 participants from 23 hospitals in Taiwan showed that 7.7% of the subjects are HLA-B* 15:02 positive. These subjects carrying HLA-B* 15:02 were then advised to take alternative drugs other than carbamazepine [39]. Consequently, taking the alternative drug greatly reduced the change of developing SCARs, especially SJS/TEN. Based on the findings from these studies, the genetic screening of HLA-B* 15:02 prior to the use of carbamazepine for certain Asian populations are recommended by different health regulatory agencies [40].

HLA-B* 15:02 association and carbamazepine-induced SJS/TEN is also proposed to be ethnic specific. It is likely due to different genetic background as the allele frequency varies among different populations. It is relatively high in Han Chinese (0.057-0.145), Malaysians (0.12-0.157), and Thai (0.085-0.275) compared to Japanese (0.002), Koreans (0.004), and Europeans (0.01-0.02) [41-47].

In the populations with lower frequency of HLA-B* 15:02, that is, Northern Europeans, Japanese, and Koreans, more recent genome-wide association studies (GWAS) showed that HLA-A* 31:01 allele has relatively stronger association with carbamazepine-induced hypersensitivity (OR = 25.93, 10.8, and 7.3 in the three populations, resp.) [41, 48-50]. In addition, HLA-B* 15:11 allele was shown to be associated with carbamazepine-induced SJS/TEN in Japanese and Korean populations as well (OR = 9.8 and 18.1 in the two populations, resp.) [41, 47]. The different strength and specificity of HLA association with carbamazepine-induced SCARs further suggest that it is necessary to perform different genetic tests for different populations.

Oxcarbazepine is also an important drug used in the treatment of epilepsy. Oxcarbazepine-induced cutaneous ADRs presented with less clinical severity including limited skin detachment (all [??] 5%) and no mortality compared to carbamazepine. Therefore, it is commonly used as an alternative to carbamazepine. A most recent study which enrolled 50 patients in Taiwan and Thailand from 2006 to 2014 identified a significant association between HLA-B* 15:02 and SJS/TEN (OR = 27.90; P =187 x [10.sup.-10]). The results of study suggested that although oxcarbazepine is used as an alternative due to the less severity of drug reactions, genetic test should also be considered further, particularly for the populations with higher frequency of HLA-B* 15:02 [51].

4.3. Allopurinol Hypersensitivity and HLA-B* 58:01 (Skin). Allopurinol is a xanthine oxidase inhibitor used in the treatment of gout and hyperuricemia. A study comparing the data in 2005 and in 2011 from Taiwan's National Health Insurance Research Database, which belongs to the nationwide population database with more than 23 million insured enrollees, demonstrated that allopurinol hypersensitivity happened in about 0.4% of the new users every year. About half of them required hospitalization [52]. Patients who underwent hospitalization had very high mortality rate (0.39/1000 new users). In 2005, the first case-control study in Taiwan showed that HLA-B* 58:01 allele is the genetic marker of allopurinol-induced SCARs in Han Chinese (OR = 580.3, P = 4.7x [10.sup.-24]) [53]. This association was then validated in different populations, such as Thailand, Japan, South Korea, Hong Kong, Australia, Portugal, and Europe [54-59]. Currently, HLA-B*58:01 is considered as a useful genetic marker for allopurinol-SCARs in multiple ethnic populations worldwide [31]. The American College of Rheumatology guideline thus recommends the HLA-B* 58:01 genetic screening for allopurinol new users in Asia populations since 2012.

A most recent study in Taiwan further enrolled a large number of patients with allopurinol-induced ADRs in order to investigate the associations between HLA-B* 58:01, renal function, gene dosage, and drug dosage with the risk of allopurinol-induced ADRs development [58]. The authors showed that HLA-B* 58:01 was strongly associated with ADRs (OR = 44.0; P = 2.6 x [10.sup.-41]) and was also highly correlated with disease severity. That is, patients carrying HLA-B* 58:01 had much higher chance to develop SCARs comparing to MPE, particularly those individuals with homozygous HLA-B*58:01. Furthermore, coexistence of HLA-B* 58:01 and renal impairment increased the risk and predictive accuracy of allopurinol-induced ADRs. This study suggests that patients with the coexistence of HLA-B* 58:01 and renal impairment should be cautious and avoid to use allopurinol.

4.4. Dapsone Hypersensitivity and HLA-B* 13:01 (Skin). Dapsone alone or in-combination with other drugs are effective for the treatment or prevention of infectious diseases (e.g. leprosy, malaria and pneumocystis pneumonia). However, about 0.5-3.6% of persons who were treated with dapsone developed hypersensitivity reactions. A recent genome-wide association study involving 872 participants (39 participants showed dapsone hypersensitivity syndrome and 833 controls) identified that SNP rs2844573, located between the HLA-B and MICA loci, was significantly associated with the dapsone hypersensitivity (OR= 6.18; P = 3.84 x [10.sup.-13]) [60]. The authors further confirmed that HLA-B* 13:01 is associated with the dapsone hypersensitivity (OR = 20.53; P = 6.84 x [10.sup.-25]). The allele showed a sensitivity of 85.5% and a specificity of 85.7% for dapsone hypersensitivity from this study and thus can be used as a marker of dapsone hypersensitivity. However, the hypersensitivity has not been studied in other ethnic populations.

4.5. Amoxicillin-Clavulanate-Induced DILI and HLA Haplotypes. Amoxicillin-clavulanate (AC) is one of the most commonly prescribed antimicrobial drugs worldwide. However, it is a known cause of DILI and accounts for 10-13% of hospitalizations. Hautekeete et al. first reported a strong association between HLA and AC-induced DILI in Europeans [61]. The authors observed a much higher frequency of DRB1* 15:01-DRB5*01:01-DQB1* 06:02 haplotype in patients with AC-induced DILI compared to normal healthy controls (57.1% in cases versus 11.7% in controls, P < [10.sup.-6]). The association was further validated in two UK populations (OR = 2.3 and 9.3 for the two populations, resp.) [62,63]. A recent study by performing GWAS in 201 patients further confirmed the association of AC-induced DILI with DRB1* 15:01 allele (OR = 4.2; P = 4.6x[10.sup.-10]) [64]. In addition, the study further identified two novel HLA alleles as risk factors of AC-induced DILI: HLA-A* 02:01 in all patients (OR = 2.2; P =1.8x [10.sup.-10]) and HLA-B* 18:01 with nominal significance independently of HLA-A* 02:01 and HLADQB1* 06:02 in Spanish patients only.

4.6. Flucloxacillin-Induced DILI and HLA-B* 57:01 Association. Flucloxacillin is an antibiotic belonging to penicillin class and is used widely for the treatment for staphylococcal infection in Europe. Flucloxacillin is a common cause of DILI and is also reported to be associated with cholestatic liver disease. A GWAS study enrolling 51 patients showed a strong association between flucloxacillin-induced DILI and a marker, rs2395029[G]. This marker is in complete linkage disequilibrium with HLA-B*5701 (P =8.7x[10.sup.-33]) [65]. The authors further performed MHC genotyping and confirmed the association of flucloxacillin induced DILI with HLA-B*5701 (OR = 80.6, P = 9.0 x [10.sup.-19]). This is an interesting finding because HLA-B*57:01 is also associated with abacavir hypersensitivity, but these patients were not reported to develop liver injury. It still remains unclear whether it resulted from the binding of different drugs/metabolites to the same HLA allele and subsequent initiation of immune responses or it is merely a coincidental event. As the positive predictive value of HlA-B*57:01 is as low as 0.12% [31], the genetic screening for HLA-B* 57:01 before the prescription of flucloxacillin to new users may not be clinically relevant.

4.7. Antithyroid Drug-Induced Agranulocytosis and HLA-B* 38:02-HLA-DRB1* 08:03 Haplotype. Other than skin and liver injures, drug reactions could also affect the immune system directly. Antithyroid drugs (ATDs) have been the cornerstones treatment of Graves' disease (GD), which is the leading cause of hyperthyroidism. It has been reported that ATDs may induce agranulocytosis resulting in lower number of white blood cells and is likely to be life threatening. However, the genetic risk factors have not been identified until recently. Chen et al. conducted both classic genotyping and GWAS to elucidate the genetic association between ATD-induced agranulocytosis and HLA genes in Taiwan [16]. First of all, they performed direct HLA genotyping including 6 classical loci for a total of 42 agranulocytosis cases and about 1200 GD controls. The results showed strong associations of ATD-induced agranulocytosis with two alleles: HLA-B* 38:02 (P = 675 x [10.sup.-32]) and HLA-DRB1* 08:03 (P =183 x [10.sup.-9]), which are in independent LD blocks. From GWAS, two more markers were further identified in the genomic region of HLA genes (6q21): rs17193122 (P = 4.29 x [10.sup.-27]), which is in LD block with HLA-B* 38:02, and rs116869525 (P = 127 x [10.sup.-8]). The two markers are in the same LD block with HLA-DRB1* 08:03. The authors further showed that the patients who carried both alleles have much higher chance to develop agranulocytosis compared to those who had only one allele. This is an interesting finding similar to the observation in amoxicillin-clavulanate-induced DILI: class I and class II HLA confer genetic susceptibility to the same drug adverse effect, as we mentioned above.

5. Different Techniques Used to Screen HLA Alleles or Predict Hypersensitivity Reactions in New Drug Users

As the association between HLA alleles and the chance of developing SCARs has been shown in many studies, it is important and advised to have the genetic test for new users of the drugs mentioned above. Systematic and large-scale genetic testing is mostly available for HLA-B*57:01 through commercial laboratories in the US as this allele has the highest frequency in Caucasians. These kits typically offer single allele testing with a short turnaround time. The genotype results are either "positive" (HLA-B*57:01 being present in one or both copies of the HLA-B gene) or "negative" (no copies of HLA-B*57:01 are present). There are no intermediate phenotypes because HLA-B is expressed in a codominant manner [27]. Although most of the technologies were developed based on the purpose of detecting HLA-B* 57:01 allele, the concept can also be applied to test other alleles. Therefore, in the following paragraph, we summarize the technologies developed to genotype HLA on the purpose of screening new drug users to avoid potential ADRs (Table 2).

5.1. PCR-Based Assays. Sequence-specific oligonucleotide (SSO) assays for HLA typing was one of the first PCR-based HLA typing methods [66, 67]. The technique amplifies a particular HLA gene locus such as HLA-A, HLA-B, or HLA-DRB1. Primers are generally designed in exons 2 and 3 for HLA class I and exon 2 for HLA class II--regions known to carry the most variations. Amplifications of all the alleles of a particular HLA locus can be performed in one PCR tube. PCR products of a particular HLA locus is then hybridized with labelled oligonucleutides specifically to a particular HLA allele or a group of alleles. Recently, several commercial kits have been developed based on SSO but can get the results in a shorter period of time such as LIFECODES HLA-B SSO Typing Kit (Immucor Transplant Diagnostics).

However, with the very high number of possible heterozygous HLA allele combinations, SSO is not sufficient to resolve all ambiguities as the method does not distinguish between cis and trans polymorphisms. Therefore, when the subjects are HLA-B*57 positive, sequence specific primer- (SSP-) PCR will be advised to further determine the specific genotype [68, 69]. Comparing to SSO, SSPPCR has higher resolution and sensitivity as it uses sequence-specific primers.

More recently, new assays were developed for HLAB* 57:01 typing on a quantitative polymerase chain reaction (qPCR) platform [70-72]. This enables detection of primer specificity through differentiating Cq values by SYBR Green quantitative (q)PCR or analysis of allele-specific PCR by high-resolution melting. Implementation of these assays on a qPCR platform significantly decreases the processing and reaction time as well as reagent costs. Jung et al. further designed primers and probes based on DNA polymorphisms using hydrolysis probes (oftentimes referred to TaqMan technology) [73]. In their study, not only the primers but also the probes were designed for generating PCR products specifically from the HLA-B*57:01 allele. Although these primers may also generate products from other HLA-B alleles that do not induce hypersensitivity reactions, hydrolysis probes can differentiate these products and only give fluorescence signals if the HLA-B* 57:01 allele is present. To reduce false-positive detection, additional probes are incorporated into a single multiplex reaction. The authors also developed PCR-restriction fragment length polymorphism (RFLP) assay for genotyping HLA-B* 57:01. In this assay, two pairs of primers, one specific to 57:01 allele and another pair is for control, selectively amplify genomic DNA followed by digestion with restriction enzymes NlaIII or RsaI. PCR products amplified from two different pairs of primers resulted in different sizes of fragments that can be visualized easily on the agarose gel.

5.2. Non-PCR-Based Techniques. Using monoclonal antibody to differentiate alleles HLA-B* 57 and HLA-B* 58 was first proposed by Kostenko et al. [74]. Monoclonal HLA-B17 antibodies (mAb 3E12), which recognized both HLA-B*57 and HLA-B* 58 allotypes (members of the group specificity, HLA-B17), was labelled with phycoerythrin while antiCD45 labelled with FITC were incubated with blood from subjects. Lymphocytes were gated based upon scatter and CD45 bright expression, and mean fluorescence intensity for HLA-B17 expression was then measured by flow cytometry. Although this is an inexpensive and rapid approach to detect the presence of two allotypes, it is proposed to be less specific and sensitive than PCR-based approaches. The subjects who test positive by mAb screening are recommended to proceed with high-resolution gold-standard typing, such as SSO and SSP-PCR, to ascertain the presence of HLA-B* 5701 or HLA-B* 5801.

Patch testing is also used to predict hypersensitivity reaction of abacavir [75] and carbamazepine [76]. Giorgini and others performed patch testing on 100 subjects including 20 cases who had experienced a hypersensitivity reaction when treated with highly active antiretroviral therapy including abacavir. Among the cases with positive patch testing results, about 50% of them carry HLA-B* 57:01 allele. More recently, Lin et al. proposed to use patch testing to predict carbamazepine induced hypersensitivity. They showed that about 60-70% of the cases who developed SJS/TEN and DRESS to carbamazepine had positive reactions in the patch testing. Although drug patch testing is a safe and inexpensive method for the identification of hypersensitivity, the sensitivity and specificity is not as good as PCR-based approaches.

6. Conclusion

In this review, we summarize the HLA alleles associated with ADRs induced by different drugs. From the literature, we learned that most of the HLA-associated ADRs have ethnic specificity. It is likely due to the different allele frequency between populations. Gonzalez-Galarza et al. summarize the allele frequencies of all the HLA genes and showed that the frequencies differ a lot [77]. For example, HLA-B* 57:01 has the highest frequency in Ireland, but has the lowest frequency in Cuba (African populations). The frequencies can of each allele in different populations be found in the public database ( [78].

Other than the HLA-associated ADRs being ethnic specific, there are also two interesting questions: (1) why one locus contributes to different ADRs as we have observed on HLA-B* 57:01 in abacavir hypersensitivity and flucloxacillin-induced DILI. (2) How different loci contribute to the same ADRs as we have seen in antithyroid drug-induced agranulocytosis and amoxicillin-clavulanate-induced DILI. As class I and class II HLA genes have different structures, cell-type distributions, and functional roles in the immune system, the genetic susceptibility from both classes for a phenotype are expected to be intriguing. How both class I and class II HLA genes confer genetic susceptibility to the same ADR requires further pathophysiological investigations.

ADR:     Adverse drug reactions
HLA:     Human leukocyte antigen
DRESS:   Drug reaction with eosinophilia and systemic symptoms
SCAR:    Severe cutaneous adverse drug reactions
SJS:     Stevens-Johnson syndrome
TEN:     Toxic epidermal necrolysis.

Conflicts of Interest

The authors declare no conflict of interest.

Authors' Contributions

Wen-Lang Fan, Meng-Shin Shiao, Rosaline Chung-Yee Hui, Shih-Chi Su, Chuang-Wei Wang, and Ya-Ching Chang contributed to the conception and writing of the manuscript. Wen-Hung Chung reviewed the manuscript. Wen-Lang Fan and Meng-Shin Shiao contributed equally to this work.


This work was supported by grants from the National Science Council, Taiwan (MOST101-2628-B-182-001-MY3, MOST103-2321-B-182-001, MOST103-2325-B-182A-004, MOST104-2325-B-182A-006, MOST105-2325-B-182A-007, and MOST104-2314-B-182A-148-MY3), and grants from Chang Gung Memorial Hospital (CLRPG2E0051-3, CMRPG290051-3, CMRPG3D0351-3, CMRPG-3D0361-3, CMRPG1F0111, CORPG3F0041-2, OMRPG2C0021, and OMRPG3E0041).


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Wen-Lang Fan, (1,2) Meng-Shin Shiao, (3) Rosaline Chung-Yee Hui, (2,4) Shih-Chi Su, (1,2,4) Chuang-Wei Wang, (2) Ya-Ching Chang, (2) and Wen-Hung Chung (1,2,4,5,6)

(1) Whole-Genome Research Core Laboratory of Human Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan

(2) Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Linkou, Taipei, Taiwan

(3) Research Center, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand

(4) Chang Gung Immunology Consortium, Chang Gung Memorial Hospital and Chang Gung University, Taoyuan, Taiwan

(5) Department of Dermatology, Xiamen Chang Gung Hospital, Xiamen, China

(6) College of Medicine, Chang Gung University, Taoyuan, Taiwan

Correspondence should be addressed to Wen-Hung Chung;

Received 1 September 2017; Accepted 24 October 2017; Published 23 November 2017

Academic Editor: Mahboobeh Mahdavinia
Table 1: Drug-induced ADRs and HLA allele associations.

Drug                                  HLA allele

Abacavir                              B * 57:01

Carbamazepine                         B * 15:02

                                      A * 31:01

                                      B * 15:11

Allopurinol                           B * 58:01

Dapsone                               B * 13:01
Phenytoin                             B * 15:02

Lamotrigine                           A * 31:01
                                      B * 15:02
Nevirapine                           DRB1 * 01:01
                                      B * 14:02
Sulphamethoxazole                       B * 38
Methazolamide                   B * 59:01, CW * 01:02
Amoxicillin-clavulanate       DRB1 * 15:01-DQB1 * 06:02
Flucloxacillin                        B * 57:01
Lumiracoxib                          DRB1 * 15:01
Ticlopidine                           A * 33:03
Antithyroid drugs               B * 38:02-DRB1 * 08:03

Drug                             Phenotype              Population

                                                     African American
Abacavir                            HSS                 Brazilian
                                                       Han Chinese
Carbamazepine                     SJS/TEN                  Thai
                                                       Han Chinese
                             MPE, HSS, SJS/TEN          Caucasian
                                  SJS/TEN                Japanese
                                                       Han Chinese
Allopurinol                       SJS/TEN               Caucasian
                                   SCARS                Taiwanese
Dapsone                             HSS
Phenytoin                         SJS/TEN              Han Chinese
Lamotrigine                         HSS                  British
                                  SJS/TEN              Han Chinese
Nevirapine                         DRESS            Hispanics, African
                                    HSS                 Sardinian
Sulphamethoxazole                 SJS/TEN                European
Methazolamide                     SJS/TEN          Korean and Japanese
Amoxicillin-clavulanate             DILI                Caucasian
Flucloxacillin                      DILI                Caucasian
Lumiracoxib                         DILI              Not available
Ticlopidine                         DILI                 Japanese
Antithyroid drugs             Agranulocytosis           Taiwanese

Drug                        Reference

Abacavir                       [79]
                             [35, 82]
Carbamazepine                  [37]
                             [49, 82]
                             [47, 84]
Allopurinol                    [57]
Dapsone                        [60]
Phenytoin                      [83]
Lamotrigine                    [86]
Nevirapine                     [87]
                             [88, 89]
Sulphamethoxazole              [57]
Methazolamide                  [84]
Amoxicillin-clavulanate        [64]
Flucloxacillin                 [65]
Lumiracoxib                    [90]
Ticlopidine                    [91]
Antithyroid drugs              [16]

Table 2: Available genetic tests.

Platform                        Technology                 Specificity

PCR              Sequence specific oligonucleotides (SSO)      >95%
PCR                 sequence-specific primer (SSP) PCR         >97%
Real-time PCR           Hydrolysis probe (TaqMan)              >99%
Flow cytometry     HLA-B17 specific monoclonal antibody        ~80%

Patch testing                                                 60-70%

Platform                       Advantage                   References

PCR                    Commercial kits available            [66, 92]
PCR                      More specific than SSO           [66, 68, 69]
Real-time PCR    Mismatch in the probe region seems to        [73]
Flow cytometry       be more sensitive than those in          [93]
                             the primer region
Patch testing             Safe and inexpensive              [75, 76]
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Author:Fan, Wen-Lang; Shiao, Meng-Shin; Hui, Rosaline Chung-Yee; Su, Shih-Chi; Wang, Chuang-Wei; Chang, Ya-
Publication:Journal of Immunology Research
Article Type:Report
Geographic Code:9TAIW
Date:Jan 1, 2017
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