key: cord-349010-n4s8dzgp
authors: Al-Tawfiq, Jaffar A.; Memish, Ziad A.
title: Update on therapeutic options for Middle East Respiratory Syndrome Coronavirus (MERS-CoV)
date: 2016-12-24
journal: Expert Rev Anti Infect Ther
DOI: 10.1080/14787210.2017.1271712
sha: 
doc_id: 349010
cord_uid: n4s8dzgp

Introduction: The Middle East Respiratory Syndrome Coronavirus (MERS-CoV) is an important emerging respiratory pathogen. MERS-CoV resulted in multiple hospital outbreaks within and outside the Arabian Peninsula. The disease has a high case fatality rate, with the need for a therapeutic option. Areas covered: In this review, we provide an overview of the progress in the development of therapeutic strategies for MERS. We searched PubMed, Embase, Cochrane, Scopus, and Google Scholar, using the following terms: ‘MERS’, ‘MERS-CoV’, ‘Middle East respiratory syndrome’ in combination with ‘treatment’ or ‘therapy’. Expert commentary: There are multiple agents tried in vitro and in vivo. None of these agents were used in large clinical studies. Available clinical studies are limited to the use of the combination of interferon and other agents. These clinical studies are based solely on case reports and case series. There are no prospective or randomized trials. There is a need to have prospective and randomized clinical trials for the therapy of MERS-CoV. However, this strategy might be hampered by the sporadic cases outside the large hospital outbreaks.

The Middle East respiratory syndrome coronavirus (MERS-CoV) emerged as an important virus in 2012 and since then has caused multiple outbreaks in hospitals especially in the Kingdom of Saudi Arabia and outside the Arabian Peninsula [1] [2] [3] . Since the emergence of MERS-CoV, a total of 1800 cases including 640 deaths were reported by the World Health Organization (WHO) [4] . Due to the increased morbidity and mortality of MERS-CoV infection, the attention was directed toward the development of prevention strategies and the establishment of therapeutic modalities. An earlier review was based on the severe acute respiratory syndrome (SARS) experience and had suggested few possible options for the treatment of MERS-CoV infection [5] . In this review, we provide an overview of the progress in the development of therapeutic strategies for MERS.

We searched PubMed, Embase, Cochrane, Scopus, and Google Scholar using the following terms: 'MERS,' 'MERS-CoV,' 'Middle East respiratory syndrome' in combination with 'treatment' or 'therapy. ' We also reviewed the references of each article to further include other studies or reports not identified by the search. We classified the studies into the following categories: in vivo and in vitro studies, animal studies, and human case reports or case series.

For clinical studies, we graded the level of the evidence based on the 'Oxford Centre for Evidence-based Medicine' [6] .

In vitro studies showed variable activity of various agents against MERS-CoV (Table 1) . These agents include: interferon, ribavirin, HIV protease inhibitors (nelfinavir, ritonavir, and lopinavir).

Interferon is antiviral type I IFN system, a major part of the innate immune response [7, 8] . In vitro studies showed that IFN-β has an IC 50 of 1.37 U/mL and that IFN-β has anti-MERS-CoV activity of 16-, 41-, 83-, and 117-fold higher than IFN-α2b, IFN-γ, IFN-universal type 1 and IFN-α2a, respectively [9] . In vitro studies showed that IFN-β has a lower IC50 for MERS-CoV compared to IFN-a2b [9] .

Ribavirin is a nucleoside analog that is activated by host kinases to a nucleotide [7, 10, 11] . It was shown that in vitro doses of ribavirin required to inhibit MERS-CoV replications are too high to be achieved in vivo [7, 10] . Nelfinavir and lopinavir inhibit MERS-CoV in vitro [7, 12] . The mean 50% effective concentration (EC50) of lopinavir using Vero E6 and Huh7 cells was 8.0 μM [13] .

Camostat and the heptad repeat 2 peptide (HR2P) are two MERS-CoV fusion inhibitors that were tested in vitro [14, 15] . The fusion inhibitor, camostat, inhibited viral entry into human bronchial submucosal gland-derived Calu-3 cells but not the immature lung tissue [14] . The second fusion inhibitor, HR2P, inhibits MERS-CoV replication and the spike protein-mediated cell-cell fusion [15] .

Cyclosporin affects the function of many cyclophilins that act as chaperones and facilitate protein folding [16, 17] . In vitro, cyclosporine inhibited MERS-CoV replication [16, 17] . Nitazoxanide, a broad-spectrum antiviral agent, and teicoplanin, an inhibitor of cathepsin L in the late endosome/lysosome and blocker of the entry of MERS-CoV, also showed inhibitory effect of MERS-CoV in vitro [18, 19] .

There are few studies evaluating various agents as therapy for MERS-CoV in animal models (Table 2) [12, [21] [22] [23] [24] . In the rhesus macaques model, interferon-α2b-ribavirin combination decreased viral replication within 8 h of MERS-CoV infection [25] . In a primate model, the mortality rate at 36 h post-inoculation was reduced from 67% in untreated to 0-33% in animals treated with a combination of interferon-β1b and either lopinavir or ritonavir [12] . Intranasal use of an HR2P analog with improved pharmaceutical property, HR2P-M2, was protective in mice model [21] . In an animal model using MERS-CoV infected mice, the use of high titer MERS immune camel serum was effective in reducing lung injury and acceleration of virus clearance [22] . Mycophenolate has a direct and indirect antiviral activity by modulation of IFN response [20] . The use of mycophenolate in the common marmoset animal model resulted in higher mortality than untreated animals [12] . A monoclonal antibody designated as m336 is an antibody derived from a large phage-displayed antibody library from B cells of healthy donors [26] . The use of this m336 in mice showed promising results as a therapeutic and a prophylactic agent [23] .

Currently, there is no animal model that completely reflects the course of MERS-CoV disease in humans and thus the data obtained from these animal models are to be interpreted cautiously. And animal models utilize therapy shortly after infection.

Based on analysis of SARS data, interferon-ribavirin combination was suggested as a possible therapeutic option for the treatment of MERS-CoV infections [5] . Limited data are available regarding the clinical efficacy of antiviral agents [27] [28] [29] [30] [31] [32] [33] [34] [35] [36] ( Table 3 ). The first use of the combination of ribavirin-interferon therapy was in five patients with MERS infection [27] . The therapy was started late in the course of the disease with a median time from admission to therapy of 19 days [27] . Of the included 5 patients, none responded to therapy [27] .

In a subsequent retrospective cohort study, 20 MERS patients received ribavirin-interferon compared to 24 patients who did not [28] . The 14-day survival rate was better in those who received the combination therapy (70% vs. 29%, p = 0.004); however, the 28-day survival rate was not statistically different (30% vs. 17%) ( Table 1 ) [28] . In another case series, 11 MERS patients had ribavirin and peg-interferon α-2a [29] .

Ribavirin-IFN-α2a was compared to ribavirin-IFN-β1a in a study of 13 and 11 patients, respectively [30] . The mortality rate was not statistically different between the two groups (85% vs. 64%) [30] . In a large cohort study of 51 patients, various combinations of interferon and ribavirin were used with different outcomes (Table 3 ) [31] . In a case series of 6 patients, 3 patients received ribavirin and interferon-alfa 2b within 1-2 days of admission and they survived compared to the other 3 patients who died as they received the therapy 12-19 days after admission [36] . Another study evaluated the use of interferon beta, interferon alpha, or ribavirin and showed survival rates of 18/23 (78.3%), 6/8 (75%), and 13/19 (68.4%), respectively (Table 3 ) [31] . The combination therapy was also used in other case reports (Table 3 ) [33, 34] . The role of the combination of ribavirin and IFN was also tried as a treatment and a prophylaxis [34] . The current studies of the use of ribavirin and IFN combination therapy for MERS-CoV infection rely on small number of patients but there is a trend for improvement. Thus, it was suggested that the combination of type 1 interferon and ribavirin could be used [37] . Due to the inhomogeneous nature of available studies and the limited data that are available, a precise recommendation on therapy of MERS could not be established.

The combination of lopinavir/ritonavir, ribavirin and interferonalpha was used in one case [32] . One patient received pegylated interferon, ribavirin, and lopinavir/ritonavir from day 13 of illness and the patient had continued MERS-CoV in the respiratory tract secretions until the fourth week of illness [33] . However, viremia was detected for only 2 days after initiation of triple therapy [33] . In a case series, eight patients received mycophenolate mofetil and all survived [31] .

In the SARS epidemic, passive immunotherapy with neutralizing antibodies was considered as a therapeutic approach. There are multiple antibodies against MERS-CoV [38] [39] [40] [41] [42] [43] [44] [45] [46] [47] [48] (Table 4 ). In the MERS-CoV infection, the production of large quantities of MERS-CoV neutralizing human polyclonal antibodies was possible using gamma-irradiated whole-killed virion vaccine or a spike protein nanoparticle vaccine in a bovine model [49] . Utilizing one dose of these antibodies prevented infection in mice [49] . These antibodies were effective when given 12 h before or 24 and 48 h after MERS-CoV infection [49] .

Corti et al. isolated a potent MERS-CoV-neutralizing antibody (LCA60) from memory B cells of an infected individual. The LCA60 antibodies bind to a site on the spike protein and neutralize MERS-CoV infection [48] . These LCA60 antibodies were used successfully in mice model [48] . Similarly, utilizing a humanized mouse model of MERS-CoV infection, antibodies against the spike protein were efficacious as prophylaxis [39] . Antibodies obtained from the sera of MERS immune camels were supportive of the clearance of the virus, and reduction of the severity of the disease in MERS-CoVinfected mice [22] . However, the purification and safety of these antibodies in humans has not been established yet.

The cellular dipeptidyl peptidase IV (DDP IV; known as CD26 or adenosine deaminase (ADA)-complexing protein-2) [48] is an important receptor that mediates MERS-CoV infection through the viral spike (S) protein [46, 50] . The MERS-CoV receptor binding domain (RBD), present on the surface spike protein (S), binds to the host cells receptor DPP IV [46, 50, 51] . In humans, DPP IV is present mainly on the lower respiratory tract area such as the bronchial epithelial and alveolar cells [52, 53] . Although DDP IV is important for the viral entry into host cells, the use of DPP IV inhibitors, sitagliptin, vildagliptin, and saxagliptin, does not block the infection of MERS-CoV [50] .

In vitro use of monoclonal antibodies (MERS-4) exhibited IC50 of 0.056 µg/mL [43] . Other possible human mAb (m336, m337, and m338) neutralize pseudovirus and live virus [45] . In rhesus model of MERS-CoV infection, a human monoclonal antibody, 3B11-N, against MERS-CoV was effective in reducing the pathology of MERS-CoV [47] . The use of polyclonal antibody (pAb) against CD26 inhibits MERS-CoV infection in vitro [50] . Humanized anti-CD26 monoclonal antibodies (MAb) such as MAb YS110 and 2F9 significantly inhibit MERS-COV infection in vitro [38] . Polyclonal antibodies against the MERS-COV S1 domain neutralize the virus infection [46] . Many other MERS-CoV antibodies are being developed and tested [38] .

In the SARS epidemic, convalescent plasma was thought to improve the outcome of SARS patients [5] . Previous studies suggest that convalescent plasma may be used for patients with SARS and severe influenza and may result in decreased viral load and a lower mortality rate [54] [55] [56] [57] . However, most of the studies were of low or very low quality, lacked control groups, and had risk of bias [58] . Two patients with MERS-CoV infection received intravenous immunoglobulin in an attempt to treat the infection, one patient was in Saudi Arabia [59] and the other was in the USA [60] . A protocol for the use of convalescent plasma as a therapeutic option for MERS was suggested [61] . Plasma donors were identified as those with anti-MERS-CoV indirect immunofluorescence assay (IFA) antibodies (titer of ≥1:160) with no evidence of active MERS-CoV infection [61] . In nine confirmed survivors of MERS-CoV infection, 55%, 33%, and 22% of them had positive MERS antibodies by IFA at 3, 10, and 18 months, respectively [62] . The two patients who had long lasting antibodies had severe disease; however, the titer of the IFA antibodies was not measured in the study [62] . In a larger study, MERS-CoV neutralizing antibodies were produced at low levels and were short-lived [63] . Further studies of the kinetics of the MERS-CoV antibodies showed that all surviving patients and 50% of fatal cases produced IgG and neutralizing antibodies [64] . The presence of antibodies did not lead to the elimination of virus from the lower respiratory tract [64] . In a study of 12 patients from South Korea, nine patients had PRNT50 titers >1:320 by day 21 and two had titers >1:320 by day 28 [65] . In a study of 443 samples, 12 (2.7%) had reactive ELISA results, and 9 of those had reactive indirect fluorescent antibody and microneutralization assay titers [66] . Thus, the use of convalescent plasma for the treatment of MERS-CoV in a clinical trial may be challenging due to a small pool of potential donors with sufficient antibody titers [66] .

Based on SARS experience, some authors suggested that steroid therapy might be beneficial for severe MERS-COV infection [67] . Corticosteroid use for patients with SARS showed that early use of corticosteroids significantly increased viral load, and 20.7-fold increase in risk of ICU admission and mortality [68] . In another study of 16 non-ICU patients, the median time for SARS-CoV to become undetectable in plasma was 12 days compared to 8 days in patients who did and did not receive early corticosteroid therapy [69] . Corticosteroids were used as adjunct therapy for many patients with MERS-CoV [27, 70] . In a study of 13 patients with MERS-CoV infection, one patient received steroid and intravenous immunoglobulin for thrombocytopenia [59] . Initial study of five patients, three patients received a combination of interferon and ribavirin in addition to adjunct steroid on day 0-21 and all died during hospitalization [27] . However, steroids were not evaluated systematically as therapy for MERS patients.

The host protease, furin, is an important factor to break down the S1-S2 region of the MERS-CoV [71] . In vivo studies showed activity of multiple agents against MERS-CoV and include: chloroquine, chlorpromazine, cyclosporine, and mycophenolic acid [7, 72] . In addition, the US FDA approved repurposed agents with broad antiviral activity including in vitro activity against MERS-CoV [73] . These agents include the polymerase inhibitor BCX4430 and the helicase inhibitor SSYA10-001, spike binding (immunoadhesin (DPP4-Fc)) [73] . There are many other agents currently in preclinical investigation such as: fluspirilene, thiothixene, fluphenazine hydrochloride, promethazine hydrochloride, astemizole and chlorphenoxamine hydrochloride [72] .

The emergence and continued cases of MERS-CoV infection require the availability of MERS therapy. There is an urgent need for the development of standardized animal models and the establishment of standardized clinical therapeutic protocols. The current clinical studies are limited to case reports and case series with no control arm. The quality of evidence these studies offer is too low to make a conclusion. It is difficult to draw conclusion in the face of these limited studies. The most used combination of therapy was interferon and ribavirin as developed initially in 2013. The development of novel therapeutic agents or the repurposing old therapeutic agents against MERS-CoV are needed as alternative pathways for testing and clinical trials. It was thought that convalescent sera may provide an exciting alternative as a therapeutic agent; the present data does not support the wide adaptation of this therapy. The current MERS therapy relies on supportive care and providing circulatory and ventilation support.

It is expected that the development and the use of repurposed drugs would allow the development of therapeutic agents for MERS-CoV. The best location to provide a randomized controlled trail was thought to be the intensive care units for the use of convalescent sera; the presence of milder disease may necessitate the development of therapeutic protocols for patients with severe and those with milder disease. Monoclonal and polyclonal antibodies may offer further therapeutic options for the disease in humans. Since the prospect for a randomized clinical trial is low due to the sporadic nature of the disease outside hospital outbreaks, it is prudent to have well-conducted prospective clinical studies. The proteins involved in MERS-CoV entry and replication are attractive targets for the development of antiviral therapeutics. Clinical studies utilizing anti-MERS-CoV antibodies as therapeutic options would add to the prospect to develop therapeutic agents for this syndrome. Although many drugs appear to be effective in vitro, a consideration of their availability, pharmacokinetic/pharmacodynamic properties, and side effects should be taken into consideration. Of medications with an attractive use, lopinavir, interferon, and mycophenolate are among these agents. Accelerated and preferably randomized controlled trails should be conducted. Neutralizing antibodies are also promising and the use of these agents in humans. Targeting the DDP4 receptor may be of particular importance; however, it is important to keep in mind that the development of any mutation in the binding sites may limit the use of these agents [74] . Few monoclonal antibodies showed protective efficacy as a prophylaxis in animal models [39, 48] . The development and testing of monoclonal antibodies are associated with high costs and lack of an undefined population for their use [75] . These monoclonal bodies had not been used in phase 1 clinical trials and that further development of these agents require time and cost.

• MERS-CoV emerged in 2012 and has caused multiple hospital outbreaks. 

This paper was not funded.

Managing MERS-CoV in the healthcare setting

• A review of MERS-CoV in healthcare setting

Hospital outbreak of Middle East respiratory syndrome coronavirus

Middle East respiratory syndrome coronavirus in healthcare settings

Middle East respiratory syndrome coronavirus (MERS-CoV) n d

Therapeutic options for Middle East respiratory syndrome coronavirus (MERS-CoV)-possible lessons from a systematic review of SARS-CoV therapy

Oxford centre for evidence-based medicine -levels of evidence

Broad-spectrum antivirals for the emerging Middle East respiratory syndrome coronavirus

Interferons and viruses: an interplay between induction, signalling, antiviral responses and virus countermeasures

Interferon-β and mycophenolic acid are potent inhibitors of Middle East respiratory syndrome coronavirus in cell-based assays

• A study of the inhibitors of MERS-CoV

Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin

Future treatment strategies for novel Middle East respiratory syndrome coronavirus infection

Treatment with lopinavir/ ritonavir or interferon-β1b improves outcome of MERS-CoV infection in a nonhuman primate model of common marmoset

• A primate model of MERS-CoV infection

Screening of an FDA-approved compound library identifies four small-molecule inhibitors of Middle East respiratory syndrome coronavirus replication in cell culture

Middle East respiratory syndrome coronavirus (MERS-CoV) infection mediated by the transmembrane serine protease TMPRSS2

Structure-based discovery of Middle East respiratory syndrome coronavirus fusion inhibitor

MERS-coronavirus replication induces severe in vitro cytopathology and is strongly inhibited by cyclosporin A or interferon-α treatment

Cyclosporin A inhibits the replication of diverse coronaviruses

Nitazoxanide, a new drug candidate for the treatment of Middle East respiratory syndrome coronavirus

Glycopeptide antibiotics potently inhibit cathepsin L in the late endosome/lysosome and block the entry of ebola virus, Middle East respiratory syndrome coronavirus (MERS-CoV), and severe acute respiratory syndrome coronavirus (SARS-CoV)

Mycophenolic acid augments interferon-stimulated gene expression and inhibits hepatitis C virus infection in vitro and in vivo

Protective effect of intranasal regimens containing peptidic Middle East respiratory syndrome coronavirus fusion inhibitor against MERS-CoV infection

Passive immunotherapy with dromedary immune serum in an experimental animal model for Middle East respiratory syndrome coronavirus infection

Passive transfer of A Germline-like neutralizing human monoclonal antibody protects transgenic mice against lethal Middle East respiratory syndrome coronavirus infection

Single-dose treatment with a humanized neutralizing antibody affords full protection of a human transgenic mouse model from lethal Middle East respiratory syndrome (MERS)-coronavirus infection

Treatment with interferon-alpha 2b and ribavirin improves outcome in MERS-CoVinfected rhesus macaques

Junctional and allele-specific residues are critical for MERS-CoV neutralization by an exceptionally potent germline-like antibody

Ribavirin and interferon therapy in patients infected with the Middle East respiratory syndrome coronavirus: an observational study

The first study of interferon and ribavirin in MERS-CoV

Ribavirin and interferon alfa-2a for severe Middle East respiratory syndrome coronavirus infection: a retrospective cohort study

•• A large cohort study of ribavirin-interferon in MERS-CoV patients

Acute management and longterm survival among subjects with severe Middle East respiratory syndrome coronavirus pneumonia and ARDS

IFN-α2a or IFN-β1a in combination with ribavirin to treat Middle East respiratory syndrome coronavirus pneumonia: a retrospective study

Treatment outcomes for patients with Middle Eastern respiratory syndrome coronavirus (MERS CoV) infection at a coronavirus referral center in the Kingdom of Saudi Arabia

Combination therapy with lopinavir/ ritonavir, ribavirin and interferon-alpha for Middle East respiratory syndrome: a case report

Virological and serological analysis of a recent Middle East respiratory syndrome coronavirus infection case on a triple combination antiviral regimen

Ribavirin and interferon-α2b as primary and preventive treatment for Middle East respiratory syndrome coronavirus: a preliminary report of two cases

Middle East respiratory syndrome coronavirus during pregnancy

Middle Eastern Respiratory Syndrome corona virus (MERS CoV): case reports from a tertiary care hospital in Saudi Arabia

Guidelines for the laboratory diagnosis of Middle East respiratory syndrome coronavirus in Korea

Inhibition of Middle East respiratory syndrome coronavirus (MERS-CoV) infection by anti-CD26 monoclonal antibody

Pre-and postexposure efficacy of fully human antibodies against spike protein in a novel humanized mouse model of MERS-CoV infection

A truncated receptor-binding domain of MERS-CoV spike protein potently inhibits MERS-CoV infection and induces strong neutralizing antibody responses: implication for developing therapeutics and vaccines

A conformation-dependent neutralizing monoclonal antibody specifically targeting receptor-binding domain in Middle East respiratory syndrome coronavirus spike protein

A humanized neutralizing antibody against MERS-CoV targeting the receptor-binding domain of the spike protein

Potent neutralization of MERS-CoV by human neutralizing monoclonal antibodies to the viral spike glycoprotein

Identification of human neutralizing antibodies against MERS-CoV and their role in virus adaptive evolution

Exceptionally potent neutralization of Middle East respiratory syndrome coronavirus by human monoclonal antibodies

The receptor binding domain of the new Middle East respiratory syndrome coronavirus maps to a 231-residue region in the spike protein that efficiently elicits neutralizing antibodies

3B11-N, a monoclonal antibody against MERS-CoV, reduces lung pathology in rhesus monkeys following intratracheal inoculation of MERS-CoV Jordan-n3/2012

Prophylactic and postexposure efficacy of a potent human monoclonal antibody against MERS coronavirus

Human polyclonal immunoglobulin G from transchromosomic bovines inhibits MERS-CoV in vivo

Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC

Molecular basis of binding between novel human coronavirus MERS-CoV and its receptor CD26

Dipeptidyl-peptidase IV from bench to bedside: an update on structural properties, functions, and clinical aspects of the enzyme DPP IV

The multifunctional or moonlighting protein CD26/DPPIV

Convalescent plasma treatment reduced mortality in patients with severe pandemic influenza A (H1N1) 2009 virus infection

Meta-analysis: convalescent blood products for Spanish influenza pneumonia: a future H5N1 treatment?

Successful treatment of avianorigin influenza A (H7N9) infection using convalescent plasma

Successful treatment of avian influenza with convalescent plasma

The effectiveness of convalescent plasma and hyperimmune immunoglobulin for the treatment of severe acute respiratory infections of viral etiology: a systematic review and exploratory meta-analysis

Clinical course and outcomes of critically ill patients with Middle East respiratory syndrome coronavirus infection

Clinical and laboratory findings of the first imported case of Middle East respiratory syndrome coronavirus (MERS-CoV) into the United States

Feasibility, safety, clinical, and laboratory effects of convalescent plasma therapy for patients with Middle East respiratory syndrome coronavirus infection: a study protocol

Antibody response and disease severity in healthcare worker MERS survivors

Transmission of MERScoronavirus in household contacts

Viral shedding and antibody response in 37 patients with Middle East respiratory syndrome coronavirus infection

•• A study of viral shedding of MERS-CoV

Kinetics of serologic responses to mers coronavirus infection in humans

Feasibility of using convalescent plasma immunotherapy for MERS-CoV infection, Saudi Arabia

Clinical recommendations from an observational study on MERS: glucocorticoids was benefit in treating SARS patients

The use of corticosteroid as treatment in SARS was associated with adverse outcomes: a retrospective cohort study

Effects of early corticosteroid treatment on plasma SARS-associated coronavirus RNA concentrations in adult patients

State of knowledge and data gaps of Middle East respiratory syndrome coronavirus (MERS-CoV) in humans

Mechanisms of coronavirus cell entry mediated by the viral spike protein

Repurposing of clinically developed drugs for treatment of Middle East respiratory syndrome coronavirus infection

Development of medical countermeasures to Middle East respiratory syndrome coronavirus

Towards the prophylactic and therapeutic use of human neutralizing monoclonal antibodies for Middle East respiratory syndrome coronavirus (MERS-CoV)

• A study of use of human neutralizing monoclonal antibodies for MERS-CoV

Research and development activities for Middle East respiratory syndrome: The Current Landscape. n d

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.