Genetic Manipulation Strategies for β-Thalassemia: A Review

Introduction

Thalassemia, an autosomal recessive hematologic disease is becoming a serious health problem worldwide with its high prevalence and incidence (1). Thalassemia is a condition in which one of the genes that code for the adult hemoglobin components, the α-and β-globin chains, are altered or missing. The globin genes can be affected by a variety of mutations, resulting in thalassemia. The β-globin gene (HBB), which exclusively encodes for β-globin chains, is reduced or missing in β-thalassemia. β-thalassemia is prevalent in Mediterranean countries, the Middle East, Central Asia, India, Southern China, and the Far East as well as countries along the north coast of Africa and in South America. Around 1.5 percent of the world's population (80 to 90 million people) is estimated to be β-thalassemia carriers, with a yearly incidence of symptomatic β-thalassemia individuals of 1 in 100,000 people globally (2).

The severity of β-thalassemia is described as three main forms: thalassemia major, thalassemia intermedia and thalassemia minor. Thalassemia major presents with severe anemia that necessitates regular red blood cell (RBC) transfusions within the first 2 years of life. Patients with untreated or inadequately transfused thalassemia major commonly experience growth retardation, pallor, jaundice, weak musculature, hepatosplenomegaly, leg ulcers, extramedullary hematopoiesis, and skeletal abnormalities as a result of bone marrow expansion. On the other hand, blood transfusions on a regular basis might lead to an excess of iron in the blood. Excess iron can cause serious and irreversible organic damage, such as cirrhosis, diabetes, heart disease, and hypogonadism, if it is not well-managed (3). The most common cause of death of β-thalassemia is secondary to cardiovascular diseases due to either severe anemia (before the era of regular blood transfusions) or iron overload (after the implementation of transfusion therapy), followed by infection (4–6).

Patients with thalassemia intermedia present later in life with moderate anemia and do not require regular transfusions. Main clinical features in these patients are hypertrophy of erythroid marrow with medullary and extramedullary hematopoiesis and its complications (osteoporosis, masses of erythropoietic tissue that primarily affect the spleen, liver, lymph nodes, chest and spine, and bone deformities and typical facial changes), gallstones, painful leg ulcers and increased predisposition to thrombosis (7). Thalassemia minor is clinically asymptomatic but some subjects may have moderate anemia with symptoms such as headache, lethargy, fatigue, dizziness, and exercise intolerance (8).

Currently, there is no other curative option for β-thalassemia except allogenic hematopoietic stem cell transplantation (HSCT). Nevertheless, this therapeutic option is not widely available for β-thalassemia patients due to the difficulty to find matched human leukocyte antigen (HLA) bone marrow donors. HSCT of mismatched HLA donor could lead to transplantation failure due to severe graft vs. host disease (GVHD) and treatment-related death (9, 10). Clinically, some studies have reported the outcomes of allogenic HSCTs application on β-thalassemia patients. A retrospective review was conducted to evaluate the clinical outcomes of allogenic HSCTs children with β-thalassemia major in a Jordan health center. Out of 34 patients included in this study, the overall survival was 97% and thalassemia free survival was 88.2% (11). In one of the health centers in Italy, a study was conducted on 80 β-thalassemia patients that received allogenic HSCTs. A total of 93.7% of patients being thalassemia-free, proving the benefit of HSCTs for most patients. Allogenic HSCT is still associated with GVHD (12.7%), graft failure (10%), and mortality (3.8%) (12). The autologous HSCT approach primarily serves as a promising therapy to cure β-thalassemia, however, there are some major challenges such as controlling transgene expression, which ideally should be erythroid-specific, differentiation stage-restricted, elevated, position independent, and sustained over time (13).

The availability of new tools and techniques in recent years has accelerated the development of gene-editing treatments to ameliorate the pathophysiology in β-thalassemia patients. In this review, we provide an overview of the genome therapeutic approaches for the β-thalassemia, including RNA manipulation therapy, splice-switching, gene editing and generation of corrected induced pluripotent stem cells (iPSCs).

Molecular Basis of β-Thalassemia

The quantitative reduction in β-globin production depends on the underlying molecular mechanisms. HBB mutations that result in no β-globin production leads to β⁰-thalassemia. Other mutations that impair the β-globin synthesis at a variable degree are classified as β⁺- or β⁺⁺- (“silent”) thalassemia. The quantitative reduction of β-globin causes its hemoglobin tetramer partner, α-globin to be in excess. The accumulation of free α-globin is responsible for the pathophysiology of β-thalassemia by which the degree of imbalance between α- and non-α-globin chain synthesis influences the severity of the β-thalassemia phenotype.

Some structurally abnormal β-globin variants are also quantitatively reduced, with a phenotype of β-thalassemia. To date, there are more than 1,400 hemoglobin variants that have been reported, with more than 900 variants in HBB gene (14). The most common β-globin structural variants are hemoglobin E (HbE [β26 Glu>Lys]), sickle hemoglobin (HbS [β6 Glu>Val]), and hemoglobin C (HbC [β6 Glu>Lys]) (15).

β^E (CD26) is one of the most common β-thalassemic mutations among Southeast Asians that affect β-globin pre-mRNA splicing, thus producing abnormal hemoglobin, HbE (16). During the translation of the gene into protein, introns in the pre-mRNA need to be removed through the splicing process (Figure 1). HBB mutations at the splice junctions activates the aberrant splice sites that reduces the efficiency of the normal splicing pathway, leading to the non-functional β-globin chain production that give rise to β-thalassemia. Other HBB aberrant splicing mutations are CD19 and CD27 mutations in exon 1, IVS1-5, IVS1-6, and IVS1-110 mutations in intron 1, IVS2-654, IVS2-705 and IVS2-745 mutations in the intron 2 (17). HBB carrying the cryptic splice site on coding sequence (exons) may either be translated into a β-globin variant (eg: β^E-globin, Hb Malay) or into a defective mRNA that will later be degraded in the nucleus of the cells.

FIGURE 1

Figure 1. Normal and aberrant splicing mechanisms. (A) Normal HBB produce normal pre-mRNA with intact three exons and subsequently translated into normal β-globin. (B) HBB with mutation in exon 1 that activates a de novo splice site may either produce correctly spliced or aberrantly spliced mRNA which later be translated into normal or no β-globin, respectively. (C) HBB with intron 1 mutation may activate correct or aberrant splicing pathways that give rise to normal or no β-globin, respectively. (D) Intron 2 mutation in HBB may induce correct or aberrant splicing mechanisms that yield normal or no β-globin, respectively. Red point marked the mutation location. Dashed line indicates the aberrant splicing mechanisms.

Almost 50% of the severe β-thalassemia patients worldwide were found with the underlying double heterozygosity for a β-thalassemia mutation and the β^E mutation (18). HbE/β-thalassemia has a highly varied phenotype, with many patients remaining mostly transfusion-free throughout their lives, while others are initiated on transfusion at an early age (19).

RNA Manipulation Strategies

Occurrence of aberrant splicing is one of the processes that affects β-globin synthesis in β-thalassemia even though the correct splice sites remain potentially functional. By blocking the aberrant splice sites or other sequence elements related to splicing with antisense oligonucleotides, the splicing machinery may be forced to reselect the right splice sites and drive the synthesis of β-globin mRNA and polypeptide, therefore restoring gene function.

Antisense Oligonucleotides

Antisense oligonucleotides (ASOs) are non-ionic DNA analogs possessing altered backbone linkages relative DNA or RNA that bind complementarily to nucleic acid sequences by Watson-Crick base-pairing (20). ASOs include antisense morpholino oligonucleotides (AMOs) and splice-switching oligonucleotides (SSOs). To improve the pathophysiology of β-thalassemia, the ASOs entered the erythroid progenitor cells, migrated to the nucleus, and hybridized to the aberrant splice sites to suppressed the aberrant splicing pattern of β-globin pre-mRNA. In consequence, the correct splicing was restored and increased the expression of functional β-globin (Figure 2).

FIGURE 2

Figure 2. How ASOs work to correct the aberrant splicing. In the presence of ASOs targeted at the mutation on the gene, the correction of aberrant splicing of human β-globin occurs and leads to the production of functional β-globin protein. Boxes indicate exons; lines, introns; red dots, mutation.

Aberrant splicing mutations in intron 2 of the HBB include mutations at nucleotides 654, 705, or 745 (β^IVS2−654, β^IVS2−705 and β^IVS2−745-globin). A cytosine to thymine mutation at nucleotide 654 of human β-globin intron 2 (β^IVS2−654) is one of the most common mutations causing β-thalassemia in Chinese and Southeast Asians that affect β-globin pre-mRNA splicing (21). In a study, erythroid progenitor cells derived from β-thalassemia major (IVS2–745/IVS2–745 and IVS2–745/IVS2–1) and β-thalassemia intermedia (IVS2–654/β^E) were treated with AMOs which targeting at the aberrant splice sites in the β-globin gene. This results in efficient restoration of correctly-spliced β-globin pre-mRNA and subsequently increase the level of hemoglobin A (HbA), suggesting the potential clinical application of AMOs to correct the aberrant splicing of β-thalassemia (22).

Furthermore, free uptake of AMOs in transgenic mice harboring IVS2-654 HBB has resulted in restoration of correct human β-globin mRNA in the erythroid cells of the transgenic mice. The effects of free uptake of AMOs were also tested on erythroid precursor cells derived from IVS2–654/β^E-thalassemia patients and as a response, increased levels of β-globin mRNA and hemoglobin A was recorded. Thus, these findings indicate the potential of restoring the β-globin mRNA splicing via free uptake of AMOs (23).

In another experiment, IVS2-654 in intron 2 of HBB was repaired in a study by Svasti and her colleague using an in vivo mouse model of IVS2–654 thalassemia. The aberrant splice site in the pre-mRNA was targeted using SSOs. Significant amounts of hemoglobin were restored in the peripheral blood of the IVS2-654 mouse, suggesting a promising alternative to correct the aberrant splicing of IVS2-654 mutation in β-globin (24).

HeLa cells that are stably expressing β^E/IVS1-6 were established by Suwanmanee et al. (25). They utilized this cell line as a tool to correct the aberrant splicing of β^E/IVS1-6 by using AMOs. Interestingly, the treatment of AMOs increased the amount of correctly spliced β^E-globin mRNA in a dose-dependent and sequence-specific manner. It was quite promising when application of the same AMOs to erythroid progenitor cells from two HbE/β-thalassemia increased the production of β^E-globin mRNA and HbE by 70 and 36%, respectively (25).

To support the previous findings, El-Beshlawy et al. (26) studied ex vivo correction of aberrant β^IVS1−110-globin pre-mRNA splicing by ASOs. A total of 10 peripheral blood mononuclear cells were derived from 10 β^IVS1−110 thalassemia patients. Fifty percent of the cases showed correction of the aberrant splicing; 2 of them showed corrected mRNA band with no aberrant mRNA band while another 3 showed increased ratio between corrected to aberrant mRNA band. In addition, significant increase of total hemoglobin level was also observed in those five corrected cases, suggesting that antisense oligomers are applicable for treating β-thalassemia (26).

Another aberrant splicing mutation of β-thalassemia, IVS2-745 (C>G) located in intron 2 of HBB, causes a premature in-frame termination codon that inhibits β-globin production. The aberrant splicing in the pre-mRNA was reversed using uniform 2'-O-methoxyethyl (2'-MOE) SSOs resulting in up to 80% increase of adult hemoglobin in erythroid cells of β^IVS2−745-thalassemia patients. Moreover, the balance between β-like and α-globin chains was restored, thus leading to reduction of toxic heme aggregates up to 87%. These findings suggest the potential application of 2'-MOE SSOs to restore the aberrant splicing in β-thalassemia patients in future (27).

Successful repair of β-globin pre-mRNA splicing defect by synthetic ASOs in erythroid cells was demonstrated. The advantages of antisense treatment include; (1) ASOs correct splicing of pre-mRNA that is transcribed from the native β-globin locus thus precluding overexpression of β-globin mRNA, (2) the approach offers a pharmacological treatment, easier to implement than gene therapy, and (3) the treatment may be easily stopped if any undesirable effects are observed (22). ASOs, however, possess inherent drawbacks. Its clinical application is limited by short-term effectiveness and the requirement for lifelong periodic administration of the ASOs to maintain therapeutic levels of β-globin (21). Moreover, this approach is not applicable to β-thalassemia with other genotypes and is limited in comparison to gene therapy, which may replace or supplant any mutant with a correct gene (22).

U7 snRNA

Engineering of viral vector mediated expression of U7 snRNA carrying the ASOs that restores the correct splicing of HBB potentially overcomes the short-term effectiveness of ASOs treatment. Small nuclear RNAs that are rich in uridine are known as U snRNAs and are numbered in order of discovery. The spliceosomes, large complexes that catalyze splicing, are divided into major and minor spliceosomes: U1, U2, U4, U5, U6 and U11, U12, U4atac, U5atac and U6atac snRNP, respectively. Although the U7 snRNP is not involved in splicing, it is a critical element in the processing of replication-dependent histone (RDH) pre-mRNAs at their unique 3' end. Furthermore, findings based on modified U7 snRNP (U7 Sm OPT) targeting splicing to induce efficient skipping or inclusion of specified exons have demonstrated U7snRNA as a useful tool in therapeutic trials. In U7 Sm OPT-based therapy, an antisense oligonucleotide is incorporated into the U7 snRNA, forming modified U7 small nuclear ribonucleoproteins (U7 snRNP) (Figure 3) (28).

FIGURE 3

Figure 3. Modified U7 snRNP. Complexes of spliceosome proteins (green) combine with U7 snRNA that is incorporated with antisense oligonucleotides targeted to the aberrant splice site of the gene. Boxes represent exons and introns.

Vacek et al. (29) transfected the HeLa cells expressing the mutations at nucleotides 654, 705 and 745 in intron 2 of HBB with modified U7 snRNA (U7.623) to prevent the aberrant splicing activated by the mutations. U7.623 that contains antisense sequence was able to reduce the incorrect splicing of the β-globin pre-mRNA and increase the level of correctly-spliced β-globin mRNA. Application of U7.623 in hematopoietic stem cells and erythroid progenitor cells derived from IVS2-745/IVS2-1 β-thalassemia patients resulted in approximately 25-fold increase in the levels of correctly-spliced β-globin mRNA and hemoglobin A. These findings proved the lentiviral vector-based gene therapy for β-thalassemia (29).

A modified U7 snRNA targeting the IVS2-654 β-globin pre-mRNA was delivered by lentivirus into iPSCs derived from mesenchymal stromal cells of a patient with HbE/β^IVS2−654-thalassemia. The efficiency of the modified U7 snRNA was proven with the high level of correctly spliced β-globin mRNA in erythroblasts differentiated from the transduced iPSCs. The modified U7 snRNA has great potential to provide the autologous iPSCs transplantation to restore the aberrant splicing of β-thalassemia (30).

An engineered U7 snRNA targeted to several pre-mRNA splicing elements on the β^IVS2−654-globin pre-mRNA, U7.BP + 623, was effective in a HeLa cell line carrying the IVS2-654 by which the correctly-spliced β^IVS2−654-globin mRNA was increased. Progenitor cells derived from HbE/β^IVS2−654-thalassemia patients were transduced with lentiviral-mediated U7.BP + 623 and promoted restoration of correct splicing of β^IVS2−654-globin mRNA as well as restoration of HbA production. This finding marked the potential usage of the lentiviral-mediated engineered U7 snRNA as an alternative for the long-term treatment of β-thalassemia (21).

A following research was performed to evaluate the effect of U7.BP+623 on β^IVS2−654-globin pre-mRNA splicing in β^IVS2−654-thalassemia mice erythroid progenitor cells. As expected, the correction of β-globin pre-mRNA splicing was achieved. However, the level of correctly spliced β-globin was lower than previously reported in patient. This situation was probably due to an inefficient processing of U7 snRNA in mouse thus producing truncated engineered U7 snRNA. The different processing of U7 snRNA in humans and mice has therefore restricted the depth analysis of the engineered U7 snRNA in the mouse model (31).

In an attempt to correct the aberrant splicing of CD26 mutation, Preedagasamzin et al. (32) proved that the U7 bE4þ1 snRNA lentiviral vector was effective in restoring the correctly-spliced β^E-globin mRNA for at least 5 months. Application of the same lentiviral vector in erythroid progenitor cells from HbE/β-thalassemia patients also resulted in the increase of the correctly-spliced β^E-globin mRNA thus suggesting the long-term treatment for the HbE/β-thalassemia patients using the engineered U7 snRNA lentiviral vector (32).

The strategy of the engineered U7 snRNA that is reported here may be a new alternative approach for β-thalassemia gene therapy, even though improvements of the vector system are still required (21). Additionally, the engineered U7 snRNA mediated splicing correction can be implemented in numerous other diseases caused by RNA mis-splicing (32).

Genome Manipulation Strategies

Recent advancements that permitted seamless engineering of the human genome using variety of technologies are collectively referred to as gene editing. Precision gene editing technologies enable the alteration of the genome at precise loci, resulting in targeted genomic changes that are being used in a variety of medical applications. The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 (Cas9) system is a widely used tool for genome engineering, however it is not the first of its kind. Zinc-finger nucleases (ZFNs) and transcription activator–like effector nucleases (TALENs), for example, are programmable protein-based genome engineering tools that have been widely used. In terms of design and cost, ZFNs are challenging. To test the cutting efficiency of TALENs, many pairs must be made. Furthermore, DNA methylation and histone acetylation may have an impact on their effectiveness. CRISPR/Cas9, on the other hand, is not limited by these constraints, is practical, and is simple to manufacture. The major goals of gene therapy are to transfer a healthy copy of HBB or to re-establish the expression of γ-globin, and hence fetal hemoglobin (HbF) (33, 34).

Genome editing using designer nucleases results in the formation of DNA double-strand breaks (DSBs) at particular genomic loci. DSBs can be repaired in the cell via homology-directed repair (HDR) and non-homologous end joining (NHEJ). HDR is a high-fidelity repair pathway that permits a homologous DNA donor template to be integrated at a particular location and potentially being exploited to correct disease-causing mutations. The error-prone NHEJ mechanism has mostly been used to generate minor insertions and deletions in order to achieve permanent gene inactivation and disruption of gene expression (Figure 4).

FIGURE 4

Figure 4. Gene editing by designer nucleases. ZFNs, TALENs, and CRISPR/Cas9 mediated the genome modifications through two main double strand break repair pathways. Indel mutations resulted from NHEJ pathway. Gene correction, insertion and replacement using DNA donor template are the outcomes of HDR pathway. FokI, endonuclease from Flavobacterium okeanokoites; PAMs, protospacer adjacent motifs; NHEJ, non-homologous end joining; HDR, homology-directed repair; dsDNA, double-stranded DNA; ssODN, single strand oligodeoxynucleotides.

ZFNs and TALENs

ZFNs are composed of three to six zinc-fingers that bind DNA sequences and a cleavage domain, FokI, to generate DSBs. In the last decade, studies have demonstrated efficient targeted integration in HSPCs by ZFNs expression with exogenous homologous recombination donors delivered via single-stranded oligonucleotides (35), integrase-defective lentiviral vectors (36), or recombinant adeno-associated viral vectors of serotype 6 (rAAV6) (37, 38). Nevertheless, research on the use of ZFNs in editing HBB gene is limited due to challenges in developing the ZFNs. As FokI-dependent DNA cleavage requires dimerization of the cleavage domains, two ZFNs are required for binding DNA (on both strands and in opposite direction) to align FokI domains and allow DNA cleavage (39). Furthermore, laboratory procedures are time-consuming without a ZFNs specialist, resulting in a large amount of effort being required to generate a successful edit. One of the key advantages of the ZFN system is the utilization of dimerized FokI, which can improve the specificity of DNA targeting while simultaneously reducing off target effects. Notably, a developed ZFN is already in the clinical trial stage, ST-400 that targets BCL11A, a master regulator of the fetal-to-adult hemoglobin switch (NCT03432364, https://clinicaltrials.gov/). Detailed informations of ZFN-mediated clinical trials are listed in Table 1. The preliminary results of a phase 1/2 clinical study in transfusion-dependent β-thalassemia patients showed a relatively low genome editing efficiency associated with poor HbF expression (40).

TABLE 1

Table 1. Clinical trials using the ZFN-mediated technology (https://clinicaltrials.gov/).

TALENs are chimeric proteins that contain two functional domains: a DNA-recognition transcription activator-like effector (TALE) and a nuclease domain. TALENs serves as customizable restriction enzymes that recognize a specific sequence and introduce an overhang double-stranded break. TALENs are considerably easier to design compared to ZFNs, thus explaining their widespread use.

Ma et al. (41) combined the integration-free β-thalassemia induced pluripotent stem cells (iPSCs) derived from patients and TALEN-based universal correction of β-globin mutations in situ. This robust process has successfully corrected the HBB and the corrected iPSCs can be induced to differentiate into hematopoietic progenitor cells and then further to erythroblasts expressing normal β-globin. This finding suggests the efficient and promising strategy to correct different types of β-globin mutations in β-thalassemia iPSCs (41).

TALENs were also being used to investigate the efficiency of correcting the aberrant splice sites in homozygous erythroblast derived from IVS1-110(G>A)-homozygous patient. As a result, significant correction at RNA, protein and morphological levels were observed, suggesting the disruption of aberrant regulatory elements by TALENs as a highly efficient gene therapy approach for suitable mutations (42).

In a study to compare between TALENs and CRISPR/Cas9, Xu et al. (43) designed both endonucleases targeting at IVS2-654 mutation in β-globin of patient-derived iPSCs. Different frequencies of double-strand breaks (DSBs) at IVS2-654 were observed when using TALENs and CRISPR/Cas9 in which TALENs have higher gene targeting efficiency. Further differentiation of TALENs-corrected iPSCs clones generated a higher transcription of β-globin compared to the uncorrected cells. These findings may guide the future application of TALENs in the treatment of β-thalassemia and other monogenic diseases (43).

In depth analysis of TALENs-mediated NHEJ correction of β-thalassemia mutation was performed in mice model carrying a IVS2-654 mutation on the β-globin gene. TALENs vectors targeting at the mutation were constructed and used to generate mice with TALENs⁺/β^IVS2−654 genotype. The sequencing analysis revealed that the IVS2-654 mutation was deleted in 50% of TALENs⁺/β^IVS2−654 mice and no off-target effects were observed. Western blot analysis confirmed the expression of normal β-globin. There are decreases in proportion of nucleated cells in the bone marrow, splenomegaly with extramedullary hematopoiesis, and iron deposition in the spleen and liver of TALENs⁺/β^IVS2−654 mice. These findings suggest a straightforward strategy to treat anemia in β-thalassemia (44).

ZFNs and TALENs have been shown to edit numerous loci in multiple cell types. While TALENs are frequently linked with less cytotoxicity than ZFNs, their larger size may constrain their delivery to therapeutically important cells for gene therapy applications. Both ZFNs and TALENs have the potential to cause off-target effects that may be detrimental to the target cells. Finally, their complex design may hinder their development for genome editing procedures (39).

CRISPR/Cas9 and Cas12a

The CRISPR/Cas9 technology was first introduced in 2012 and has resulted in a paradigm shift in the field of genome editing. The major difference between this system and other nucleases (i.e. ZFNs and TALENs) is that the Cas9 nuclease is directed to the DNA by Watson-Crick base pairing rather than a protein-DNA interaction via an RNA molecule (guide RNA, gRNA). Cas9 activity is dependent on the presence of protospacer adjacent motifs (PAMs), which are short sequences downstream of the target sequence (protospacer) that are complementary to the gRNA. PAMs are unique to the Cas9 generated from each bacterial species.

β-thalassemia iPSCs that had a CD17 (A>T) homozygous point mutation in HBB was corrected with CRISPR/Cas9 producing gene-corrected iPSCs that possess normal karyotype and maintained pluripotency without any off-targeting effects. The differentiation efficiency was evaluated and proven by the increased embryoid body ratio and various hematopoietic progenitor cells percentages. Notably, the gene-corrected β-thalassemia iPSCs restored HBB expression and reduced reactive oxygen species production compared to un-corrected group, implying that CRISPR/Cas9 system had greatly improve the hematopoietic differentiation efficiency of β-thalassemia iPSCs (45).

Xiong et al. (46) studied the combination effect of CRISPR/Cas9 and single strand oligodeoxynucleotides (ssODNs) in iPSCs derived from IVS2-654 β-thalassemia patients. CRISPR/Cas9 is targeted at the IVS2-654 mutation site on HBB and mediates the double strand breaks (DSBs). ssODNs are then seamlessly corrects the gene. The corrected iPSCs maintained the pluripotency and are able to differentiate normally, thus producing correct β-globin. The strategy of combining CRISPR/Cas9 system and ssODNs provides the promising gene correction of β-thalassemia and can be considered as future approaches for management of β-thalassemia (46).

Xu et al. (47) demonstrated the disruption of the aberrant splice site targeted at IVS1-110G>A mutation using Cas9 ribonucleoprotein (RNP) and IVS2-654C>T mutation by Cas12a/Cpf1 RNP in primary CD34+ hematopoietic stem and progenitor cells (HSPCs) from β-thalassemia patients. In regards with the high efficiency and penetration of Cas9 and Cas12a, the edited patient HSPCs showed reversal of aberrant splicing and restoration of β-globin expression. Notably, up to 73% InDel was observed and frequent 1-bp insertions at the IVS1-110 site was enough to restore normal β-globin splicing. The application of this gene editing technology offers a bright future for the treatment of transfusion-dependent β-thalassemia genotypes (47).

CRISPR/Cas9 gene editing technology was also being applied in CD34+ cells from Egyptian β-thalassemia patients with a IVS1-110 mutation. Cas9 and guide RNA were transfected into the CD34+ cells and causing DSBs at the target site and knocked out the IVS1-110 mutation. The corrected CD34+ cells gained the wild-type HBB and then were subjected for differentiation by culturing them in complete media containing erythropoietin. This study supported the existing studies for the application of CRISPR/Cas9 to treat β-thalassemia (48).

A strategy for correcting the −28 (A>G) and the 4-bp (TCTT) deletion at codons 41 and 42 in exon 2 was developed by reprogramming the patient-derived iPSCs through combination of CRISPR/Cas9 technology and the piggyBac transposon. A seamless correction of the HBB mutations through the HDR-based strategy was achieved with no off-target effects. On top of that, the cells also able to maintain their full pluripotency and exhibit normal karyotypes. After differentiation of the corrected iPSCs into erythroblasts, the gene-corrected iPSCs were successfully restored the expression of HBB compared to the parental iPSCs line. The seamless HBB correction demonstrating a critical step toward the stem cell-based gene therapy in the future (49).

Another efficient technique to correct −28(A>G) mutation was also developed by combining CRISPR/Cas9 with asymmetric single-stranded oligodeoxynucleotides (assODNs). Using K562 cell line carrying −28(A>G) mutation, the transcriptome level was compared with K562 cell line and found that the mutation disturbed the transcription and expression of β- and γ-globin gene. Interestingly, the abnormalities due to the −28(A>G) mutation were corrected by CRISPR/Cas9 and asymmetric assODNs in K562^−28(A>G). This study is the first to report on the whole-transcriptome analysis based on isogenic cell lines, thus it provides a platform to conduct future investigation of the mechanism of −28(A>G) β-thalassemia (50).

In two different groups, Liu and Niu applied CRISPR/Cas9-mediated HDR-based approaches to the iPSCs derived from β-thalassemia patients carrying 4-bp deletion (–TCTT) and (–CTTT) at CD41/42 mutation on β-globin gene respectively (51, 52). Specific CRISPR/Cas9 to target the mutation site was designed and they combined it with ssODNs. The repaired cells expressed normal β-globin transcripts when developed into hematopoietic progenitor cells and later erythroblasts. Notably, the corrected cells had a low mutational load and no off-target mutagenesis, as revealed by off-target analysis and whole-exome sequencing (52). These researches demonstrate the most efficient and safe method for genetically correcting the CD41/42 4-bp deletion in iPSCs through CRISPR/Cas9 and ssODNs to cure monogenic disease-associated mutations in patient-specific iPSCs.

The G>A point mutation in codon 26 of HBB was also corrected using guide RNA, Cas9 and ssODNs donor template via HDR-based approach. iPSCs was generated from human dermal fibroblasts of HbE/β-thalassemia patient's carrying CD41/42 mutation in one allele, and CD26 mutation in the other. After hematopoietic differentiation, the restoration of HBB protein expression was observed indicating that a single allele genetic correction of CD26 is sufficient to normalize the β-globin level in HbE/β-thalassemia. Nevertheless, only 2.9% of iPSCs clones showed efficient gene correction owing to poor transfection and HDR efficiency. The HDR efficiency might be improved by suppressing the NHEJ pathway once, however, the theory needs to be properly assessed in the future study (53).

Cosenza et al. (54) aimed to correct one of the most frequent β-thalassemia in Mediterranean area, β⁰39-thalassemia mutation, by utilizing the advanced technology of CRISPR/Cas9 gene editing. After CRISPR/Cas9 gene correction on erythroid precursor cells obtained from homozygous β⁰39-thalassemia patients, they demonstrated the presence of normal β-globin genes with high amount of normal β-globin mRNA and protein. Subsequently, the HbA level increased significantly and therefore reduce the excess free α-globin. These findings promote the development of this technique for the β⁰39-thalassemia patients and the positive outcomes may be maximized through the use of other therapeutic approaches such as reactivation of HbF (54).

Interestingly, Cai and coworkers established a novel universal approach that could potentially cure various β-thalassemia-causing mutations. This strategy is based on targeted integration of a donor template containing the complementary DNA (cDNA) that encodes the wild-type HBB gene. β-globin production was restored in erythrocytes derived from iPSCs of two transfusion-dependent β-thalassemia patients HBB that carry mutations CD17/IVS2-654 and CD17/CD41/42. This strategy of restoring functional HBB gene expression is expected to be clinically effective for permanently curing β-thalassemia patients with various HBB mutations in the future (55).

Coexistent of hereditary persistence of fetal hemoglobin (HPFH) and β-thalassemia have been long known to minimize the hematological abnormalities and result in a mild clinical manifestation. HPFH is a condition with consistently high HbF production that present in adulthood, which usually due to mutations in the β- or α-globin gene cluster or the γ promoter gene region. Ye et al. (56) mimics the HPFH genotype in bone marrow-derived adult CD34+ HSPCs by delivering target site-specific SaCas9 to remove part of β-globin locus and repaired by non-homologous end joining (NHEJ). Up to 31% of CD34+ HSPCs were successfully edited with the 13-kb HPFH5 deletion and after differentiation into erythroid cells in vitro, these cells significantly expressed the γ-globin compared to cells without HPFH deletions. Therefore, this study proved the potential new approach to autologous transplantation therapy to treat homozygous β-thalassemia (56).

One of the factors that determine the severity of β-thalassemia is the number of α-globin genes (HBA1 and HBA2) by which α-globin gene deletions ameliorate β-thalassemia through the balanced ratio of α- and β-globin. A novel strategy was developed by combining 2 therapeutic approaches mediated by CRISPR/Cas9; deletion of HBA2 gene to recreate α-thalassemia trait with reduced α-globin production and integration of β-globin transgene downstream the HBA2 promoter to increase β-globin expression. The study demonstrated the correction of the α/β-globin imbalance in erythroblast derived from edited β-thalassemia HSPCs, suggesting a novel therapeutic strategy for the treatment of β-thalassemia in the future (57).

CRISPR-Cas9 system serves some major advantages including: (1) ease of design and cloning, (2) high genome editing efficiency, (3) low cytotoxicity and transient expression when delivered as ribonucleoproteins (RNPs) versus mRNA delivery (which is typically used for ZFNs and TALENs), and (4) the possibility of multiplexing, which enables simultaneous targeting of multiple loci (58). Taken together, these benefits make CRISPR-Cas technology the optimal tool for developing therapeutic methods. To date, a number of clinical trials have been recorded to evaluate the potential of CRISPR-mediated technology in clinical settings as listed in Table 2.

TABLE 2

Table 2. Clinical trials using the CRISPR-mediated technology (https://clinicaltrials.gov/).

Conclusions

The accumulated research evidences to date demonstrate that genome editing technologies have made substantial contributions to the development of treatment options for a variety of human diseases. In the present review, we summarized the applications of different gene editing tools including ASOs, U7 snRNA, ZFNs, TALENs, and CRISPR/Cas9 systems. ASOs-driven correction of aberrant splicing is sequence and mutation specific, thus limited to certain cases of β-thalassemia. Nevertheless, some of the most common mutations that cause aberrant splicing are responsible for almost 90% of thalassemia cases worldwide (1). Hence, a small number of ASOs may be useful for treatment of a large majority of thalassemia patients. The lifelong therapeutic effect of U7 snRNA has captured the attention along with its compact size and less toxicity properties. The advancement of HDR-based DNA repair through ZFNs, TALENs, and CRISPR/Cas9-mediated double strand break has promised a potential approach to cure the β-thalassemia genetically. Nonetheless, despite the significant opportunities for therapy and translational research, as well as recent technological advancements, gene therapy still has some limitations, including design difficulties and costs associated with the use of ZFNs, TALENs, and CRISPR/Cas9, off target effects, low transfection efficiency, in vivo delivery-safety, and ethical concerns.

Author Contributions

MJ and RB: conceptualization and writing—review and editing. NZ: writing—original draft preparation. WA, AM, RA, and SS: visualization. MJ, RB, and AM: supervision. MJ: funding acquisition. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by Fundamental Research Grant Scheme (FRGS/1/2018/SKK08/USM/02/6) to MJ from the Ministry of Higher Education, Malaysia.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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