Crohn’s Disease: Comparison
Please note this is a comparison between Version 3 by Rita Xu and Version 2 by Rita Xu.

Objective: Crohn’s Ddisease is increasing in incidence and prevalence in younger people and is of a particularly aggressive nature, highlighting an urgent need for a more efficacious therapy. One such emerging therapy target. One emerging treatment targets Mycobacterium avium paratuberculosis Mycobacterium avium paratuberculosis(MAP), an organism implicated in the causation of the Crohn’s Ddisease. Therefore, this study aimed to reviewed a cohort of paediatric patients with active Crohn’s Ddisease treated with Anti-Mycobacterial Antibiotic Therapy (AMAT).

Methods: Sixteen Ppaediatric patients (n = 16) , the majority of whom had failed conventional immunosuppressive therapy, soughtwere treatmented with Anti-Mycobacterial Antibiotic TherapyMAT. Endoscopic remission was scored using the Simple Endoscopic Score for Crohn’s Disease and clinical remission was scorassessed using the Weighted Paediatric Crohn’s Disease Activity Index. Blood i (wPCDAI). Inflammatory blood markers were also routinely recorded.

Results: Patients were followed up clinically and endoscopically during treatment after an average of two months (range 1-6) and 17 months (range 2-49)–49), respectively. A significant reduction in both scores assessing clinical improvement (p < 0.001) and mucosal healing (p < 0.0078) was observed at these timepoints, where; 47% of patients had achieved clinical remission and 63% endoscopic remission. Haemoglobin and Serum Iserum inflammatory markers normalised for more than 50% of the cohort by six months of treatment. No substantial changes were observed in liver function tests and white blood cell counts and no adverse eadverse effects were reported throughout treatment.

Conclusions: This is the first report of Anti-Mycobacterial Antibiotic Therapy offering a safe and efficacious alternate therapy for paediatric patients with Crohn’s Disease. However, further larger randomised studies are required in order to validate the present findings.

  • Mycobacterium paratuberculosis
  • Crohn's disease
  • paediatric
  • mycobacterial therapy

1. DefiniAbstraction

Objective: Crohn’s dDisease is increasing in incidence and prevalence in younger people and is of a particularly aggressive naturee, highlighting an urgent need for a more efficacious therapy. One such emerging treatmentherapy targets Mycobacterium avium paratuberculosis (MAP)Mycobacterium avium paratuberculosis, an organism implicated in the causation of the Crohn’s dDisease. Therefore, this study aimed to reviewed a cohort of paediatric patients with active Crohn’s dDisease treated with Anti-Mycobacterial Antibiotic Therapy (AMAT).

Methods: Sixteen pPaediatric patients, (n = 16) the majority of whom had failed conventional immunosuppressive therapy, weresought treatedment with AMATnti-Mycobacterial Antibiotic Therapy. Endoscopic remission was scored using the Simple Endoscopic Score for Crohn’s Disease and clinical remission was assessescored using the Weighted Paediatric Crohn’s Disease Activity Index (wPCDAI). I. Blood inflammatory blood markers were also routinely recorded.

Results: Patients were followed up clinically and endoscopically during treatment after an average of two months (range 1-6) and 17 months (range 2–49),-49) respectively. A significant reduction in both scores assessing clinical improvement (p < 0.001) and mucosal healing (p < 0.0078) was observed at these timepoints, where; 47% of patients had achieved clinical remission and 63% endoscopic remission. Haemoglobin and serum iSerum Inflammatory markers normalised for more than 50% of the cohort by six months of treatment. No adverse esubstantial changes were observed in liver function tests and white blood cell counts and no adverse effects were reported throughout treatment.

Conclusions: This is the first report of Anti-Mycobacterial Antibiotic Therapy offering a safe and efficacious alternate therapy for paediatric patients with Crohn’s Disease. However, further larger randomised studies are required in order to validate the present findings.

2. Introduction

Crohn’s disease (CD) is an incurable chronic inflammatory disease occurring predominantly in the gastrointestinal tract and is characterized by deep ulceration, skip lesions, transmural inflammation, fistulae and non-caseating granulomas [1]. CD has a damaging effect on many aspects of a patient’s quality of life and has been shown to be more pronounced in paediatric patients [2][3]. Recent research suggests that newly industrialised countries account for the majority of the increase in paediatric CD incidence on a global scale [4].

Exclusive enteral nutrition (EEN) is recommended as the first line therapy for paediatric CD, with mucosal healing rates ranging from 19% to 75% [5]. Despite this, the long-term efficacy and applicability of EEN is limited with a reported relapse rate of 58% [6]. Oral corticosteroids are used for the induction of remission in moderate to severe paediatric CD cases [5]. However, their use is limited due to their inability to promote significant levels of mucosal healing in patients [7][8] and can lead to serious adverse events [5][9]. Anti-TNF (tumor necrosis factor) agents, as part of a treatment group known as biologics, can achieve mucosal healing both to a higher degree and more rapidly [10]. However, there are concerns regarding the safety and long-term effectiveness of biologics. A loss of response, mediated by the formation of antibodies, occurs in up to 36% of patients within one year of starting treatment [11]. Other notable risks associated are psoriasis, with an incidence of 16% and opportunistic infections such as sepsis, meningitis and pneumonia which have been reported in 3.3% of paediatric patients [5][12].

The sudden emergence of CD in traditionally low-prevalence regions such as Asia suggests that the development of CD may be influenced by environmental determinants [13]. One specific bacterium, Mycobacterium avium subspecies paratuberculosis (MAP), has been suggested to be a prominent environmental factor in the pathogenesis of CD [14]. Indeed, several studies have observed strong correlations between the incidence of Johne’s disease; an inflammatory granulomatous enteritis of livestock known to be caused by MAP and the rates of CD in the same geographic region [15][16][17]. These studies formed vital pieces of evidence employed by Chiodini in 2012 to describe MAP’s fulfilment of Bradford Hill’s Criteria for Causation in CD [18][19].

Recent increasing evidence about the involvement of MAP in the pathogenesis of CD has led to the development of a targeted and specialized antibiotic regimen termed Anti-Mycobacterial Antibiotic Therapy (AMAT). AMAT consists of four antibiotics, with rifabutin, clarithromycin and clofazimine the mainstay; and nitroimidazole or quinolone making up the fourth depending on the clinical presentation. Large randomized controlled studies assessing this precise antibiotic regimen were limited until a recent phase-three trial, where at week 26, 37% of patients who received standard therapy with added AMAT entered clinical remission compared to 23% in the control group who received standard therapy with the addition of a placebo [20].

The rapid rise in CD prevalence and the lack of safe and effective treatment options for children with CD prompts the need for an alternative, yet effective treatment modality. Recent evidence surrounding the pathogenic role of MAP in CD and the effectiveness of AMAT in the adult population with CD warrants further investigation into its applicability to the paediatric cohort.

3. Results

Sixteen patients (11 male), previously diagnosed with CD were identified to have started AMAT at an average age of 14 years (range: 10 years) (Table 1). The majority of patients (n = 14) had been referred to our centre due to failed previous therapies, most commonly immunosuppressive (n = 12) (Table 1).

Table 1. Demographic summary of the paediatric patients treated with Anti-Mycobacterial Antibiotic Therapy (AMAT) (n = 16).

Characteristics Value
Age and Sex  
Age at commencement (mean) 14.2
Males (n) 11
Previous Treatment  
Previous treatment (n) 14
Previous immunosuppressive treatment (n) 12
Ciprofloxacin
8 (32.5 ± 4.6)

A total of 15 patients for wPCDAI and eight for SES-CD had sufficiently detailed medical records in order to calculate retrospective scores. Prior to AMAT, the median pre-treatment wPCDAI and SES-CD scores were 47.5 (n = 15, range: 60) and 24 (n = 8, range: 27) respectively (Table 2). There was a statistically significant reduction in wPCDAI scores at the first clinical follow up appointment (p < 0.001), where seven (47%) patients achieved clinical remission (Table 2). A further seven patients reached clinical remission at subsequent clinical follow up appointments which occurred after an average of five months since the commencement of AMAT (data not shown). All eight patients scored with the SES-CD displayed a significant reduction when comparing their score prior to treatment and at their first colonoscopy during treatment (p = 0.0078). Five of these patients (63%) returned SES-CD scores indicative of endoscopic remission at their first colonoscopy after the commencement of AMAT which occurred after an average of 17 months (Table 2).

Table 2. Clinical and endoscopic remission rates for the paediatric cohort.

AMAT Drugs (
n
) and Dosage
(
σ
x
¯
Max Dose mg/kg/d) used in Combination  
Rifabutin 16 (10.9 ± 0.7)
Clarithromycin 15 (26.4 ± 2.1)
Clofazimine 16 (2.4 ± 0.2)
Metronidazole 8 (8.7 ± 0.6)

A total of nine (56%) patients were prescribed concomitant medications from a minimum of one of the following immunosuppressive drug classes: anti-TNF, steroidal, immunomodulatory and 5-ASA. Statistical analysis indicated that concomitant use of either a steroidal and/or immunomodulatory medication during AMAT did not predict clinical and endoscopic remission in such patients. There was an inadequate number of patients prescribed both Anti-TNF and 5-ASA drugs concomitantly in order to perform a Fisher’s exact test to determine a possible synergistic effect.

The median values for all three of CRP, ESR and Hb serum levels were outside the standard reference range prior to treatment (Figure 1A–C). After six months of AMAT, the median values reduced to within the normal reference ranges for all three serum markers; CRP (0–5 mg/L), ESR (1–15 mm/h) and Hb (120–160 g/L) (Figure 1A–C). Outliers in the CRP and ESR data analysis included patients experiencing secondary infections and non-compliant patients.

Figure 1. Box and whisker plots were generated in GraphPad Prism 8 under the Tukey method where the median is indicated by the horizontal bar and outliers indicated.‘·’ = The Outlier mark; more than 3/2 times of the upper quartile. The number of patients with blood results for serum C-reactive protein (CRP) (A), erythrocyte sedimentation rate (ESR) (B), hemoglobin (Hb) (C) and white cell count (WCC) (G) at pre-treatment, 1, 6 and 12 months during treatment were 16, 15, 13 and 11 respectively. The number of patients with blood results for serum alkaline phosphatase (ALP) (D) and alanine transaminase (ALT) (F) at pre-treatment, 1, 6 and 12 months during treatment were 15, 14, 12 and 10 respectively. The number of patients with blood results for serum aspartate transaminase (AST) (E) at pre-treatment, 1, 6 and 12 months during treatment were 14, 13, 11 and 9 respectively. The standard serum reference ranges for paediatric patients are indicated in grey (CRP: 0–5 mg/L, ESR: 1–15 mm/h, Hb: 120–160 g/L, ALP: 100–450 U/L, AST: 10–40 U/L, ALT: 5–30 U/L, WCC: 4.5–13.5 × 109/L).

Liver function tests (ALP, AST and ALT) as well as WCC showed no significant changes in the population within the first year of treatment (Figure 1D–F). One patient experienced continual fevers while taking rifabutin, however, these were reduced and managed via dosage modulation. Six patients contracted Clostridioides difficile infections (CDI) during AMAT, which were treated with fecal microbiota transplantation (FMT).

3. Discussion

This retrospective review reports for the first time the safety and efficacy of a combination antibiotic regime targeting MAP in paediatric patients with CD. The results of the present study successfully complement the recent Randomised Control trial (RCT) assessing the clinical efficacy of AMAT in the adult population. [20] Following our sustained antibiotic regime, we report significant rates of both clinical and endoscopic remission within our paediatric cohort with no significant adverse effects.

Our results in this small cohort indicate that AMAT may be as effective if not more than currently utilised therapies for the induction of clinical and endoscopic remission (Table 2 and Table 3). Though only 47% of patients achieved clinical remission at their first clinical follow up (Table 2), a total of 93% of patients achieved clinical remission at subsequent follow up appointments after an average of five months of treatment (data not shown). We report complete mucosal healing in 63% of our cohort at their first follow up colonoscopy during treatment (Table 2). This result is analogous to the higher rates of endoscopic remission reported in studies using Infliximab though after a longer period of treatment; 17 months compared to a range of 2.5 to 14 months (Table 2 and Table 3 respectively). 

There was marked heterogeneity within our cohort specifically surrounding the extent of and type of prior treatment (Table 1). We observed a notable trend whereby patients who had received a greater volume of immunosuppressive therapy prior to AMAT tended to respond both less rapidly and to a lesser extent when compared to those patients who had received fewer or no therapies. Interestingly, immunosuppressives have been shown to have anti-microbial activity, [28][29][30] though non-specific for MAP. Hence, one postulation is that the extent of previous immunosuppressive therapy may predict a longer duration to achieve endoscopic remission under AMAT due to the development of resistant forms of MAP in such patients. Certainly, a recent published report by our group supports this notion, in which eight treatment naïve patients experienced significant rates of both clinical and endoscopic remission at 6 weeks and 12 months respectively. [31]

Although a similar combination of antibiotics was used in our patients, a recent phase three RCT assessing the efficacy of AMAT in adult patients utilised a single capsule formulation; RHB-104, which has reported superior efficacy against MAP infections compared with the same individually dissolved drugs. [20], [32], [33] Despite this, we report greater efficacy in our paediatric cohort compared with the phase three trial in adults; clinical remission rates of 43% at the first clinical follow up (Table two) and total clinical remission rates of 93% after an average of five months (data not shown) compared with 37% at six months respectively. [20]

The antibiotics utilised within the AMAT protocol reported here are widely used and safe in paediatric patients when the dosage is adjusted for weight. A sun-tanned appearance, nausea and itchiness are the most common side effects reported in patients treated with AMAT constituents, however no such side effects were reported by our cohort. Notable, yet rarer iatrogenic effects, such as leucopenia and elevated transaminases can occur if a dose escalation model is not employed. [34][35][36] However, no significant changes in the WCC and liver function test results (Figure 1D-1G) in our patients occurred during AMAT, suggesting that the adopted dose escalation model is suitable. However, larger prospective studies conducted under controlled conditions are required to confirm these results.

A noteworthy finding of our study was the high percentage of patients experiencing CDI whilst being treated with AMAT. However, whether these infections are a result of the antibiotics perturbing the gut microbiome, rendering it susceptible to colonization remains unclear. It is unlikely that AMAT would encourage the development of CDI since multiple constituents of the therapy; specifically, Metronidazole, Tinidazole and Rifabutin are effective treatments against the infection. [37] Furthermore, paediatric IBD is reportedly associated with a higher incidence of CDI when compared to adults which may partially explain the rates of CDI observed within our cohort. [38] Despite no accounts of increased rates of CDI in previously published studies using AMAT, [20] the authors suggest that future, prospective trials examining the safety of AMAT in the paediatric cohort should take this finding into account.                                                                        

There are several recognised limitations to this study due to its retrospective design and small sample size. One significant limitation of the present study is that both wPCDAI and SES-CD scores were not calculated at the time of treatment, thus, retrospective calculation may have introduced some level of scoring bias. The lack of a suitable control population for comparison further highlights the uncontrollable limitations associated with retrospective studies and should be employed in future prospective trials. Though no significant synergistic effect was observed in patients who were prescribed concomitant immunosuppressive therapies. Larger, prospective trials should examine the effect these drugs have when used in combination with AMAT compared to AMAT alone.

The present study failed to evaluate the duration of remission in patients due to significant gaps in long term follow up data. Therefore, forthcoming RCTs should also focus on establishing the duration of both clinical and endoscopic remission compared to current treatments.

4. Conclusions

Despite a well-documented aggressive disease presentation and a recent exponential rise in the incidence of paediatric CD, fewer therapies are available in children when compared to the adult population. We examined the safety and efficacy of a combination antibiotic regime consisting of Rifabutin, Clofazimine and Clarithromycin targeting MAP, a proposed contributing factor in the pathogenesis of CD. This study provides a valuable and novel proof of concept regarding the applicability of AMAT to a broad range of clinical presentations in paediatric Crohn’s Disease patients. We report no significant side effects as a result of a dose escalated, sustained antibiotic regimen and suggest that AMAT may be more efficacious in the treatment of childhood onset compared with adult onset CD. Furthermore, we observed a notable trend, which proposes that the extent of prior immunosuppressive therapy may predict a longer treatment course with AMAT. Future targeted and more robust RCT’s should also focus on sub-populations in terms of disease severity, extent of prior treatment and the time since initial diagnosis prior to the commencement of AMAT.

References

  1. Feuerstein, J.D.; Cheifetz, A.S.; Crohn disease: Epidemiology, diagnosis, and management. Mayo Clin. Proc. 2017, 92, 1088–1103.
  2. Cohen, R.D. The quality of life in patients with Crohn’s disease. Aliment. Pharm. Ther. 2002, 16, 1603–1609.
  3. Chaparro, M.; Garre, A.; Ricart, E.; Iglesias-Flores, E.; Taxonera, C.; Domènech, E.; Gisbert, J.P.; ENEIDA study group Differences between childhood- and adulthood-onset inflammatory bowel disease: The CAROUSEL study from GETECCU. Aliment. Pharm. Ther. 2019, 49, 419–428.
  4. Ng, S.C.; Shi, H.Y.; Hamidi, N.; E Underwood, F.; Tang, W.; I Benchimol, E.; Panaccione, R.; Ghosh, S.; Wu, J.C.Y.; Chan, F.K.L.; et al. Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: A systematic review of population-based studies. Lancet 2017, 390, 2769–2778, doi:10.1016/s0140-6736(17)32448-0.
  5. Ruemmele, F.M.; Veres, G.; Kolho, K.L.; Griffiths, A.; Levine, A.; Escher, J.C.; Dias, J.A.; Barabino, A.; Braegger, C.P.; Bronsky, J.; et al. Consensus guidelines of ECCO/ESPGHAN on the medical management of paediatric Crohn’s disease. J. Crohn’s Colitis 2014, 8, 1179–1207.
  6. Cameron, F.L.; Gerasimidis, K.; Papangelou, A.; Missiou, D.; Garrick, V.; Cardigan, T.; Buchanan, E.; Barclay, A.R.; McGrogan, P.; Russell, R.K. Clinical progress in the two years following a course of exclusive enteral nutrition in 109 paediatric patients with Crohn’s disease. Aliment. Pharm. Ther. 2013, 37, 622–629, doi:10.1111/apt.12230.
  7. Canani, R.B.; Terrin, G.; Borrelli, O.; Romano, M.; Manguso, F.; Coruzzo, A.; D’Armiento, F.P.; Romeo, E.; Cucchiara, S. Short- and long-term therapeutic efficacy of nutritional therapy and corticosteroids in paediatric Crohn’s disease. Dig. Liver Dis. 2006, 38, 381–387, doi:10.1016/j.dld.2005.10.005.
  8. Borrelli, O.; Cordischi, L.; Cirulli, M.; Paganelli, M.; Labalestra, V.; Uccini, S.; Russo, P.M.; Cucchiara, S.; et al. Polymeric diet alone versus corticosteroids in the treatment of active pediatric Crohn's disease: A randomized controlled open-label trial. Clin. Gastroenterol. Hepatol. 2006, 4, 744–753.
  9. Gasparetto, M.; Guariso, G. Crohn’s disease and growth deficiency in children and adolescents. World J. Gastroenterol. 2014, 20, 13219–13233, doi:10.3748/wjg.v20.i37.13219.
  10. Nuti, F.; Civitelli, F.; Bloise, S.; Oliva, S.; Aloi, M.; La Torre, G.; Viola, F.; Cucchiara, S. Prospective Evaluation of the Achievement of Mucosal Healing with Anti-TNF-? Therapy in a Paediatric Crohn’s Disease Cohort. J. Crohn’s Colitis 2015, 10, 5–12, doi:10.1093/ecco-jcc/jjv126.
  11. Hyams, J.S.; Crandall, W.; Kugathasan, S.; Griffiths, A.; Olson, A.; Johanns, J.; Liu, G.; Travers, S.; Heuschkel, R.; Markowitz, J.; et al. Induction and Maintenance Infliximab Therapy for the Treatment of Moderate-to-Severe Crohn’s Disease in Children. Gastroenterol. 2007, 132, 863–873, doi:10.1053/j.gastro.2006.12.003.
  12. Courbette, O.; Aupiais, C.; Viala, J.; Hugot, J.-P.; Louveau, B.; Chatenoud, L.; Bourrat, E.; Martinez-Vinson, C. Infliximab Paradoxical Psoriasis in a Cohort of Children with Inflammatory Bowel Disease. J. Pediatr. Gastroenterol. Nutr. 2019, 69, 189–193, doi:10.1097/mpg.0000000000002349.
  13. Molodecky, N.A.; Soon, I.S.; Rabi, D.M.; Ghali, W.A.; Ferris, M.; Chernoff, G.; Benchimol, E.I.; Panaccione, R.; Ghosh, S.; Barkema, H.W.; et al. Increasing incidence and prevalence of the inflammatory bowel diseases with time, based on systematic review. Gastroenterology 2012, 142, 46–54.
  14. Naser, S.; Ghobrial, G.; Romero, C.; Valentine, J.F. Culture of Mycobacterium avium subspecies paratuberculosis from the blood of patients with Crohn’s disease. Lancet 2004, 364, 1039–1044, doi:10.1016/s0140-6736(04)17058-x.
  15. Fridriksdottir, V.; Gunnarsson, E.; Sigurdarson, S.; Gudmundsdottir, K.B. Paratuberculosis in Iceland: Epidemiology and control measures, past and present. Vet. Microbiol. 2000, 77, 263–267.
  16. Pickup, R.W.; Rhodes, G.; Arnott, S.; Sidi-Boumedine, K.; Bull, T.J.; Weightman, A.J.; A Hurley, M.; Hermon-Taylor, J. Mycobacterium avium subsp. paratuberculosis in the Catchment Area and Water of the River Taff in South Wales, United Kingdom, and Its Potential Relationship to Clustering of Crohn’s Disease Cases in the City of Cardiff. Appl. Env.. Microbiol. 2005, 71, 2130–2139, doi:10.1128/aem.71.4.2130-2139.2005.
  17. Greenstein, R.J. Is Crohn’s disease caused by a mycobacterium? Comparisons with leprosy, tuberculosis, and Johne’s disease. Lancet Infect. Dis. 2003, 3, 507–514.
  18. Hill, A.B. The environment and disease: Association or causation? Proc. R. Soc. Med. 1965, 58, 295–300.
  19. Chiodini, R.J.; Chamberlin, W.M.; Sarosiek, J.; McCallum, R.W. Crohn’s disease and the mycobacterioses: A quarter century later. Causation or simple association? Crit. Rev. Microbiol. 2012, 38, 52–93, doi:10.3109/1040841x.2011.638273.
  20. D. Y. Graham. Late breaking abstracts. United Eur. Gastroenterol. J. 2018, 6, 1586–1597.
  21. Greenstein, R.J.; Su, L.; Haroutunian, V.; Shahidi, A.; Brown, S.T. On the action of methotrexate and 6-mercaptopurine on M. avium subspecies paratuberculosis. PLoS ONE 2007, 2, e161.
  22. Krishnan, M.Y.; Manning, E.J.B.; Collins, M.T. Effects of interactions of antibacterial drugs with each other and with 6-mercaptopurine on in vitro growth of Mycobacterium avium subspecies paratuberculosis. J. Antimicrob. Chemother. 2009, 64, 1018–1023, doi:10.1093/jac/dkp339.
  23. Bach, H.; Rosenfeld, G.; Bressler, B. Treatment of Crohn’s disease patients with infliximab is detrimental for the survival of Mycobacterium avium ssp. paratuberculosis within macrophages and shows a remarkable decrease in the immunogenicity of mycobacterial proteins. J. Crohn’s Coliti 2012, 6, 628–629, doi:10.1016/j.crohns.2012.01.011.
  24. Agrawal, G.; Clancy, A.; Sharma, R.; Huynh, R.; Ramrakha, S.; Borody, T.J. Targeted Combination Antibiotic Therapy Induces Remission in Treatment-Naïve Crohn’s Disease: A Case Series. Microorganisms 2020, 8, 371, doi:10.3390/microorganisms8030371.
  25. Alcedo, K.P.; Thanigachalam, S.; Naser, S.A. RHB-104 triple antibiotics combination in culture is bactericidal and should be effective for treatment of Crohn’s disease associated with Mycobacterium paratuberculosis. Gut Pathog. 2016, 8, 32, doi:10.1186/s13099-016-0115-3.
  26. Qasem, A.; Safavikhasraghi, M.; Naser, S.A. A single capsule formulation of RHB-104 demonstrates higher anti-microbial growth potency for effective treatment of Crohn’s disease associated with Mycobacterium avium subspecies paratuberculosis. Gut Pathog. 2016, 8, 45, doi:10.1186/s13099-016-0127-z.
  27. Crabol, Y.; Catherinot, E.; Veziris, N.; Jullien, V.; Lortholary, O. Rifabutin: Where do we stand in 2016? J. Antimicrob. Chemother. 2016, 71, 1759–1771, doi:10.1093/jac/dkw024.
  28. Cholo, M.C.; Steel, H.C.; Fourie, P.B.; Germishuizen, W.A.; Anderson, R. Clofazimine: Current status and future prospects. J. Antimicrob. Chemother. 2012, 67, 290–298, doi:10.1093/jac/dkr444.
  29. Van Der Paardt, A.-F.L.; Akkerman, O.W.; Gualano, G.; Palmieri, F.; Forsman, L.D.; Aleksa, A.; Tiberi, S.; De Lange, W.C.; Bolhuis, M.S.; Skrahina, A.; et al. Safety and tolerability of clarithromycin in the treatment of multidrug-resistant tuberculosis. Eur. Respir. J. 2017, 49, 1601612, doi:10.1183/13993003.01612-2016.
  30. Gerding, D.N.; Muto, C.A.; Owens, R.C., Jr Treatment of Clostridium difficile infection. Clinical Infectious Diseases 2008, 46 (Suppl 1), S32–S42.
  31. Hourigan, S.K.; Sears, C.L.; Oliva-Hemker, M. Clostridium difficile infection in pediatric inflammatory bowel disease. Inflamm. Bowel Dis. 2016, 22, 1020–1025.
  32. Alcedo, K.P.; Thanigachalam, S.; Naser, S.A. RHB-104 triple antibiotics combination in culture is bactericidal and should be effective for treatment of Crohn’s disease associated with Mycobacterium paratuberculosis. Gut Pathog. 2016, 8, 32, doi:10.1186/s13099-016-0115-3.
  33. Qasem, A.; Safavikhasraghi, M.; Naser, S.A. A single capsule formulation of RHB-104 demonstrates higher anti-microbial growth potency for effective treatment of Crohn’s disease associated with Mycobacterium avium subspecies paratuberculosis. Gut Pathog. 2016, 8, 45, doi:10.1186/s13099-016-0127-z.
  34. Crabol, Y.; Catherinot, E.; Veziris, N.; Jullien, V.; Lortholary, O. Rifabutin: Where do we stand in 2016? J. Antimicrob. Chemother. 2016, 71, 1759–1771, doi:10.1093/jac/dkw024.
  35. Cholo, M.C.; Steel, H.C.; Fourie, P.B.; Germishuizen, W.A.; Anderson, R. Clofazimine: Current status and future prospects. J. Antimicrob. Chemother. 2012, 67, 290–298, doi:10.1093/jac/dkr444.
  36. Van Der Paardt, A.-F.L.; Akkerman, O.W.; Gualano, G.; Palmieri, F.; Forsman, L.D.; Aleksa, A.; Tiberi, S.; De Lange, W.C.; Bolhuis, M.S.; Skrahina, A.; et al. Safety and tolerability of clarithromycin in the treatment of multidrug-resistant tuberculosis. Eur. Respir. J. 2017, 49, 1601612, doi:10.1183/13993003.01612-2016.
  37. Gerding, D.N.; Muto, C.A.; Owens, R.C., Jr Treatment of Clostridium difficile infection. Clinical Infectious Diseases 2008, 46 (Suppl 1), S32–S42.
  38. Hourigan, S.K.; Sears, C.L.; Oliva-Hemker, M. Clostridium difficile infection in pediatric inflammatory bowel disease. Inflamm. Bowel Dis. 2016, 22, 1020–1025.
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