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      COVID-19 and the newly rediscovered multidisciplinarity

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      Immunotherapy
      Future Medicine Ltd
      anti-PD-1/PD-L1, COVID-19, immunosuppressed, immunotherapy, janus kinase inhibitors, pandemic, SARS-CoV-2, tocilizumab, virus

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          Abstract

          In the middle of the breathless fight against COVID-19, the eyes behind the facial masks of the physicians were those of either pneumologists, rheumatologists, oncologists, endocrinologists, surgeons and, in some cases, also dermatologists. This happened especially in centers heavily hurt by the SARS-CoV-2 outbreaks, involving all the hospital medical staff in the COVID-wards. Many of us have been uprooted from our quiet surgeries and day-hospitals to be catapulted into chilling emergency situations, never faced, nor imagined, during our previous professional routines. Each of us has tried to do our best, by applying a significant dose of resilience and taking hints from our original background, thus finally contributing to the imaginative therapeutic approaches rapidly emerging since the first few weeks of the pandemic. Corroborated by this scenario, the present special focus issue collects the efforts from the most disparate branches of medicine, demonstrating the heterogeneity of approaches required by COVID-19 and contributing to opening our minds to a world of possibilities, from the bench to the bedside. So it was that, taking lessons from rheumatology, several immunemodulators have been tested in the COVID-19 setting: Cala-García et al. described the efficacy of the anti-IL-6 tocilizumab against the SARS-CoV-2 infection [1], and Chang et al. reported the outcome of patients undergoing treatment with JAK inhibitors, providing suggestions from both rheumatology and dermatology [2]. Furthermore, taking the cue from cancer immunotherapy, anti-PD-1/PD-L1 immune-checkpoint inhibitors have been proposed as a possible solution to oppose the progression of the SARS-CoV-2 infection: along this line, this issue reports useful hints for research by Gatto et al. in their commentary [3]. On the other hand, oncological case series and representative cases developing COVID-19 during treatment with immune checkpoint inhibitors have been reported by Perrone et al. and by Rodrigo et al., raising the issue of the risks from SARS-CoV-2 infection in special populations [4,5]. Again, from similarities between COVID-19 cytokine storm and the cytokine-release syndrome associated with CAR-T cell therapy in hematology, antibodies against IL-6 and GM-CSF have been employed by Melody et al. in an interesting case report [6]. Even coagulopathy experts have been involved in the treatment of this difficult disease, introducing low-weight molecular heparins among the therapeutic armamentarium, due to the likely significant contribution of the vascular compartment to the pathogenesis of the illness [7]. Finally, it seems that a thin but meaningful thread links COVID-19 pathogenesis and progression with metabolic diversities, in turn subtended by individual immunological patterns, as suggested in the present issue by Finelli et al. [8], constituting a crucial environment for the clinical evolution of this viral disease. Unfortunately, SARS-CoV-2 infections often do not allow thoughtful reflections on the main components of the worsening condition of the patient, and the emergency frequently leads to messy therapeutic solutions. In the end, the same patient could have been treated with both immunesuppressants or immune-enhancers, with the aim of timely intercept of the upcoming phase of the disease. If the cruciality of the immune response in COVID-19 pathogenesis is out of the question, it is still unclear if the morbidity could be more due to an initial immune-suppressive vulnerability or, on the contrary, to a late and aberrant immune hyperactivation. The reports published in the present issue, aside from contributing to a valuable brainstorming on the underlying biological mechanisms to exploit for COVID-19 recovery, represent the testimony of the complicated rationale behind the current therapeutic approaches to the disease. If the use of tocilizumab still emerges as one of the most promising solutions, supported by scarce prospective evidence but pushed by the unmet need of an effective treatment [1,6], the attempt to outflank the immune system suppression has led to the proposal of an immuneprotection, exploiting physiological checkpoints to restore the immunocompetence [3]. It is the same rationale behind the immunotherapy of cancers, recently revolutionizing the therapeutic approach to solid tumors from an immunosuppressive perspective (e.g., chemotherapy) to an immunerestoring attempt [9]. The switch is difficult to accept, but in the case of oncology the clinical evidence strongly advocates the newest approach, likely the most physiological, relying more on the normalization than on the enhancement of the immunological status [10]. Indeed, the immune checkpoint blockade limits its effects in removing a block, allowing normal operation of the immune system to resume, more than enhancing the immune activation, that could even be harmful in the context of severe COVID-19. Aside from the treatment of the SARS-CoV-2 infection, primary and secondary prevention is an incredibly important concern, especially in frail populations such as those affected by cancer, hematologic malignancies, obesity, pulmonary chronic obstructive disease, cardiovascular diseases or metabolic disorders [2–5,8]. The first tool to be exploited for prevention is knowledge: an accurate epidemiological framework of the disease in frail populations is unfortunately still missing, given the lack of the true denominator on which COVID-cases were reported. In the current scenario, the value of reliable predictions could be even more important in the lack of prophylactic solutions, especially in light of the fact that the only effective tool applied until today was social distancing. Reliable predictions of future outbreaks, of their setting and extension, would be the only tool to prevent the evolution of events in which the world has stumbled in the last few months. In the meantime, the heartfelt research of therapeutic solutions remains a mission of physicians and researchers of all branches, sometimes contributing to creating new professional figures between immunology, infectious diseases and other specialties. Because union is strength (Figure 1). Figure 1. Multidisciplinarity in COVID-19 management.

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          A Paradigm Shift in Cancer Immunotherapy: From Enhancement to Normalization

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            From targeting the tumor to targeting the immune system: Transversal challenges in oncology with the inhibition of the PD-1/PD-L1 axis

            After that the era of chemotherapy in the treatment of solid tumors have been overcome by the “translational era”, with the innovation introduced by targeted therapies, medical oncology is currently looking at the dawn of a new “immunotherapy era” with the advent of immune checkpoint inhibitors (CKI) antibodies. The onset of PD-1/PD-L1 targeted therapy has demonstrated the importance of this axis in the immune escape across almost all human cancers. The new CKI allowed to significantly prolong survival and to generate durable response, demonstrating remarkable efficacy in a wide range of cancer types. The aim of this article is to review the most up to date literature about the clinical effectiveness of CKI antibodies targeting PD-1/PD-L1 axis for the treatment of advanced solid tumors and to explore transversal challenges in the immune checkpoint blockade.
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              Potential protective and therapeutic role of immune checkpoint inhibitors against viral infections and COVID-19

              Cancer care during COVID-19 pandemic On 11 March 2020, the WHO declared the 2019 novel coronavirus outbreak an international Public Health Emergency [1]. Cancer patients represent a particularly vulnerable population, at increased risk of COVID-19 with a worse outcome than individuals without cancer [2]. Since the US FDA approval of the CTLA-4 inhibitor ipilimumab in 2011, indications for immune checkpoint inhibitors (ICI) have dramatically expanded, becoming an effective treatment option for a wide variety of cancers, including melanoma, renal carcinoma, lung cancer, urothelial cancer and head and neck carcinoma. It is still unclear how to manage checkpoint inhibitor therapy in the context of the current emergency, due to the alleged alert of serious pneumonia in case of COVID-19 [3]. Human COVID-19 presents with a wide spectrum of clinical manifestations ranging from asymptomatic to severe disease. Respiratory epithelial cells are the primary targets for the virus and are a leading source of immunopathological injury. HLA host haplotype are fundamentally important. Clinically, the immune response induced by COVID-19 is two-phased. First, the incubation period, a nonsevere stage, during which the virus induces a protective immune response. In this phase strategies to boost immune response (antisera or pegylated IFN-α) are adopted, aimed at eliminating the virus and avoiding disease progression to severe stages. For the development of an endogenous protective immune response, a good general health status and an appropriate HLA host haplotype are fundamental. Different HLA haplotypes contribute to individual variations in defense against pathogens and are associated with distinct susceptibility to various infectious diseases. Accordingly, it seems to be advantageous to have specific HLA haplotype with increased binding specificities to the SARS-CoV-2 peptides. When the protective immune response is inadequate, the patient enters the second phase, the severe stage, characterized by strong inflammatory response, massive tissue damage especially in the lung and in organs that have high angiotensin-converting enzyme 2 expression, such as intestine and kidney [4]. The severe cases present with pneumonia which can lead to diffuse alveolar and capillary injury, pulmonary edema and acute respiratory distress syndrome, a condition that can rapidly evolve in a multiorgan failure. The pathophysiology of unusually high pathogenicity for COVID-19 has not been completely understood; one of the supposed mechanisms underlying disease severity is a hyperinduction of pro-inflammatory cytokines, known as ‘cytokine storm’ [5]. It is a vasculitic-like condition that resembles the secondary hemophagocytic lymphohistiocytosis, characterized by increased levels of IL-2, IL-7,G-CSF, IFN-γ inducible protein 10, monocyte chemoattractant protein 1, macrophage inflammatory protein 1-α (MIP1A) and TNF-α. Similar to the SARS disease, the main histological finding in COVID-19 is an exudative and proliferative lung injury, with the formation of a clear liquid jelly and hyaline membrane. Tissue-resident macrophages overactivation is implicated in the release of a storm of cytokines leading to multiorgan dysfunction, such as pancytopenia, disseminated intravascular coagulation, hepatobiliary and central nervous system dysfunction. The crux of the pathogenesis is the overproduction, by tissues macrophages, of IL-1b, which drives the acute phase response to infection, the Th17 differentiation and the immunopathogenic response observed in acute respiratory distress syndrome and COVID-19 [6]. IL-1b and TNF-α both induce TH17 cell responses and vascular permeability. The overactivation of T cells, manifested by an increase of Th17 and high cytotoxicity of CD8 T cells, accounts for, in part, the severe immune injury. TH17 cells produce IL-17 and GM-CSF, both associated with autoimmune and inflammatory disease. IL-17 promotes the production of G-CSF, IL-6, IL-1b and TNF-α that lead to systemic inflammatory symptoms, including fever. Chemokines like MIP2A, IL-8, IP10, MIP3A engage immune infiltrates [7]. IFN-γ is pleiotropic cytokine that enhances IL-6 production in monocytes and activates a large downstream cascade through the Janus kinase 1/Janus kinase 2 signaling. IL-6 promotes recruitment of neutrophils and cytotoxic T cells and has a crucial role: it inhibits the ability of lung dendritic cells to trigger naive T cells, thereby minimizing the adaptive immune response [6]. Huang et al. have performed comparison between patients who had been admitted to the intensive care unit and those who had not, observing that serum levels of IL2, IL7, IL10,G-CSF, IP10, MCP1, MIP1A and TNF-α are higher in intensive care units patients, suggesting that the cytokine storm is associated with disease severity [8]. Cancer immunotherapy works by reducing the suppression of the effector T cells, respiratory epithelial cells especially CD8+, thereby restoring the cellular immunocompetence and improving tumor-specific immune responses. The main adverse effects of immune checkpoints inhibitors are related to excessive production of pro-inflammatory cytokines IL-6 and TNF-α; the immune-mediated lung injury, termed checkpoint inhibitor pneumonitis, occurs in about 3–5% of patients receiving ICI; however, the real-world incidence may be higher, especially now that ICI are used outward of clinical trials [9]. Thus, a potential synergy between the lung toxicity from ICI and the SARS-CoV-2 related interstitial-pneumonia has been hypothesized in patients receiving anticancer immunotherapy [3]. Patients receiving ICI are in a hyperimmune condition and can develop aberrant reactions in case of COVID-19 infection due to the overlap between the two pathogenetic mechanisms of lung injury. Is it possible to estimate the risk of contracting infections of cancer patients treated with immunotherapy compared with patients treated with chemotherapy and compared with the general population? Although our observations have no epidemiological background, we are quite surprised by the limited number of patients undergoing immunotherapy contacting us due to COVID-19. Role of ICI against viral infections & SARS-CoV-2 ICIs are currently widely used in oncology due to dramatic and durable responses in a variety of tumor types, but there are few data on their possible use in the treatment of human infectious diseases. Besides immunosurveillance in cancer, the pivotal function of immune system is the protection against pathogens, bacteria, viruses and fungi. As it occurs, even in chronic viral infections, for example, HIV and HBV infection, T cells undergo a continuous lasting antigen exposure, which is the driver of a phenomenon of ‘anergy’ in T cells called T-cell exhaustion. Exhausted CD8 T cells have reduced effector function and poor proliferative capacity and their primary characteristic is the overexpression of inhibitory receptors CTLA4 and PD-1/PD-L1 [10]. The efficacy of monoclonal antibodies against PD-1 and PD-L1, that have notably revolutionized the treatment of cancer, suggests that therapeutically targeting these pathways would also be effective for preventing and treating a range of infectious diseases. Several studies have suggested that ICIs empower T-cell responses giving immunity protection during many chronic viral, bacterial or parasitic infection, including malaria, HIV infection, HBV infection and TB. In numerous mouse models of cancer and chronic infection, PD-1-targeted therapy suppresses tumor growth and reduces viral load. Similar results have been observed in primates [11]. Many clinical trials on the use of immune checkpoint blockade in chronic viral infection are designed and performed in individuals with malignancies. Gane et al. have recently published a Phase Ib study of Nivolumab (anti PD-1) with and without GS-477, an HBV therapeutic vaccine, in chronic HBV-patients. They observed that Nivolumab was well-tolerated, leading to HBsAg decline in most patients. In one patient they obtained complete HBsAg seroconversion and HBsAg loss [12]. Gay et al. reported the role of an anti-PD-L1 antibody (BMS-936559) in HIV-infected patients in a Phase II study, obtaining an enhance of HIV-1-specific immunity in most of the participants. This is the only trial of an ICI in HIV patients without cancer disease [13]. Interestingly, the inhibition of the immune checkpoint system CD200-CD200R1 has shown positive effects on coronaviruses, restoring IFN production and increasing virus clearance [14,15]. A trial with another ICI anti-PD1, Camrelizumab, is also ongoing in COVID-19 patients. Although the data from clinical trials in infectious diseases are still weak, checkpoint inhibitors are proving to have great potential in controlling viral infections and reducing viral load. Whereas on one hand the checkpoint blockade can contribute to ‘fuel’ the cytokine storm in case of coexistence of COVID-19, on the other hand, the recovery of immunocompetence could play a protective or even therapeutic role against the viral infection. We can therefore hypothesize two scenarios:  The first ‘pre-infectious phase’: the population treated with ICI is more ‘resistant’ to the attack of COVID-19;  The second ‘infectious phase’: patients receiving immunotherapy, when contracting the COVID-19, may develop more serious respiratory symptoms and complications, sustained together by the ‘cytokine storm’ and the ICI-immune mediated injury. Evidence-based guidelines on the correct management of cancer ICIs during the COVID-19 outbreak are currently lacking and experts are only providing generic practical recommendations [16–19] such as:  To delay ICI in case of durable and long-lasting responses, considering the growing evidence of a durable benefit from immunotherapy after treatment outage;  To prefer regimens with longer interval, for example, durvalumab 4-weekly administration (instead of 2-weekly), nivolumab 480 mg every 4 weeks or pembrolizumab 400 mg every 6 weeks, in order to reduce the frequency of hospital visits;  To delay durvalumab (within 42 days) for III stage lung cancer after concomitant chemoradiotherapy;  To postpone immunotherapy in case of flu symptoms, in particular fever, cough, myalgia and fatigue. All presumed cases should be tested with nasopharyngeal swab-PCR for definite diagnosis. If a patient results positive to SARS-CoV-2 and is asymptomatic, 28 days of delay and two negative tests (at 1-week interval) should be considered before restarting the treatment. The issue whether to continue or delay immunotherapy during the coronavirus outbreak is crucial, since these agents may be detrimental in the case of virus-related pneumonia, but at the same time they are quite effective and potentially curative in cancer, especially in melanoma. A multicentric registry should be strongly encouraged to understand the impact of the COVID-19 infection on cancer patients and in particular on patients undergoing immunotherapy, and to identify the risk factors for poor outcome. Conclusion The COVID-19 pandemic represents a unique challenge but also a learning opportunity. The complex immune responses for patients on immunotherapy treatment against noncancer antigens are largely unknown and giving an incorrect interpretation is a possibility. ICIs have only minimally been studied in human infectious diseases; therefore, it is not excluded that they may soon revolutionize the treatment against infectious agents, including COVID-19. Unfortunately, in the era of ICIs, the clinical advances in the oncology field are yet to be matched with those in the infectious, but there are broad perspectives for investigations and developments in future.
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                Author and article information

                Journal
                Immunotherapy
                Immunotherapy
                IMT
                Immunotherapy
                Future Medicine Ltd (London, UK )
                1750-743X
                1750-7448
                22 September 2020
                September 2020
                22 September 2020
                : 10.2217/imt-2020-0205
                Affiliations
                1Department of General and Specialistic Medicine, University Hospital of Parma, Medical Oncology Unit, Parma, Italy
                2Department of Medicine & Surgery, University of Parma, Parma, Italy
                Author notes
                [* ]Author for correspondence: bersamel@ 123456libero.it
                Author information
                https://orcid.org/0000-0002-6527-6281
                Article
                10.2217/imt-2020-0205
                7560467
                42c5d789-b906-48f3-984e-f1653e1de1cb
                © 2020 Future Medicine Ltd

                This work is licensed under the Creative Commons Attribution 4.0 License

                History
                : 11 July 2020
                : 11 September 2020
                : 22 September 2020
                Page count
                Pages: 3
                Categories
                Foreword

                anti-pd-1/pd-l1,covid-19,immunosuppressed,immunotherapy,janus kinase inhibitors,pandemic,sars-cov-2,tocilizumab,virus

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