key: cord-0708309-u1cjpwzb
authors: Kiprov, Dobri D.; Herskowitz, Ahvie; Kim, Daehwan; Lieb, Michael; Liu, Chao; Watanabe, Etsuko; Hoffman, Jan C.; Rohe, Regina; Conboy, Michael J.; Conboy, Irina M.
title: Case Report: Therapeutic and immunomodulatory effects of plasmapheresis in long-haul COVID
date: 2021-11-24
journal: F1000Res
DOI: 10.12688/f1000research.74534.1
sha: 793f33c546a25ff62c4dfd71cf3578a314c0e3c6
doc_id: 708309
cord_uid: u1cjpwzb

Many patients with COVID-19 experience a range of debilitating symptoms months after being infected, a syndrome termed long-haul COVID. A 68-year-old male presented with lung opacity, fatigue, physical and cognitive weaknesses, loss of smell and lymphocytopenia. After rounds of therapeutic plasma exchange (TPE), the patient returned to normal activities and work. Mechanistically in the patient’s peripheral blood mononuclear cells (PBMCs), markers of inflammatory macrophages diminished and markers of lymphocytes, including natural killer (NK) cells and cytotoxic CD8 T-cells, increased. Circulating inflammatory proteins diminished, while positive regulators of tissue repair increased. This case study suggests that TPE has the capacity to treat long-haul COVID.

The symptoms of "long-haul" coronavirus disease 2019 (long COVID) are debilitating and prevent patients from working, which is projected to negatively impact the healthcare system and economic recovery. 1 The most common symptoms of long COVID are dyspnea with abnormal chest radiograph (CXR) findings, extreme fatigue, cognitive impairment (described as "brain fog"), myalgias, anosmia, ageusia, headache and sleep disorder. 2 Long COVID resembles myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) which is driven by autoantibodies. 3, 4 Therapeutic plasma exchange (TPE) was successfully tried in patients with severe COVID-19 5 and is typically used on patients with ME/CSF and other autoimmune disorders. 6, 7 Moreover, our recently published studies suggest that TPE re-sets the circulatory proteome to healthier states, attenuating the so-called cytokine storm and enhancing the systemic determinants of tissue repair. 8, 9 The encouraging results of these reports convinced us to try TPE on a patient with severe long COVID.

A 68-year-old caucasian male attorney, who reported having been very physically active and capable of multitasking in a demanding executive position at work began to feel fatigued and short of breath on December 14, 2020. He visited an emergency room on December 18, 2020. His oxygen saturation was 90-93% on room air and he was sent home. His breathing and fatigue deteriorated, so he was admitted to the hospital on December 21, 2020. He tested positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by PCR and was treated with remdesivir and Decadron (dexamethasone). His status continued to worsen, and he was placed on high-flow oxygen. He was never intubated. After 11 days in the hospital, he was sent home on portable oxygen which he used intermittently.

Over the following four weeks, he felt extremely fatigued. He could only walk to the bathroom and back to bed. He could not focus on anything cognitively, which he described as "brain fog". He was unable to do any work and could not even answer his emails. He reported he had no sense of smell nor taste. Sedimentation rate, CRP, D-dimer and ferritin were abnormal in clinical lab tests ( Figure 1B ). At that time, chest radiographs and a chest CT scan revealed ground-glass appearance areas diffusely spread throughout his lungs ( Figure 1C) . A PCR test for SARS-CoV-2 was negative. A serologic test for anti-SARS-COV-2 IgG antibodies was positive.

In February of 2021, he was seen in our clinic. At that time, he was very weak and unable to walk. When he arrived at the airport, he needed a wheelchair to go from the plane to the taxi. He underwent his first TPE on February 4, 2021. One plasma volume was exchanged, using 5% albumin as an exchange fluid. The removed plasma was very dark and opaque ( Figure 1D ). During his first TPE treatment, he was coughing profusely. After his first treatment, he could breathe more easily, and the cough subsided. The morning after the first TPE treatment, he could walk and was not struggling for breath. Two days later, he had no difficulty breathing and was able to walk 100 feet on a level surface but still had difficulty walking uphill.

He underwent a second TPE and two days after the second treatment he was able to walk uphill with ease and even jog. His brain fog disappeared, and he was able to get back to his daily work activities. Typical biomarkers of systemic inflammation all became quickly and robustly normalized including erythrocyte sedimentation rate, CRP, ferritin, and D-dimer 10 ( Figure 1B ). The plasma from the second TPE was clear ( Figure 1D ). A week later his chest radiographs showed considerable clearing of the opacities in the lungs ( Figure 1C ). He also reported regaining his sense of smell and taste. He was seen in the clinic for another TPE two months later and, at that time, the patient reported that he was back to work, feeling like his normal self, and able to exercise daily without shortness of breath.

The peripheral blood mononuclear cells (PBMC) and blood serum of this patient were collected and analyzed before the first round of TPE (R0) and before each subsequent round (R1-R3) ( Figure 1A ). Real-time qRT PCR was used to study the levels of the markers of T cells: CD3; helper T-cells: CD4; cytotoxic T-cells: CD8; NK cells: CD94; B-cells: B220 and CD19; macrophages: CD11b; inflammatory myeloid cells: CD68; and IL-2 receptor: CD25. Before TPE, there was a prevalence of CD68+ inflammatory myeloid cells' marker, and relatively fewer lymphocyte markers, which is indicative of a lack of adaptive immunity ( Figure 2 ). TPE increased the markers of T-cells, B-cells, NK cells, and diminished the markers of inflammatory macrophages, suggesting enhanced adaptive immunity and attenuated inflammatory response ( Figure 2 ). CD3, CD4 and CD19 initially diminished at 5 days after the first TPE, R1, but then steadily increased during the longer intervals of R2 and R3; CD94 and CD8, the markers of cytotoxic immune cells that combat viral infections also gradually and steadily increased ( Figure 2 ).

Five days after the first TPE and the initial increase of CD11b+, the levels of this marker stabilized, while the CD68 marker of inflammatory macrophages were never elevated by TPE and were diminished by R2 and R3 (Figure 2 ). Plotting the ratios of T-cell and B-cell markers to myeloid and inflammatory macrophage markers (CD11b and CD68) demonstrates a rapid and robust shift toward adaptive immunity through the rounds of TPE ( Figure 2 ). The effects of TPE are particularly striking when looking at the relative increase in the CD8+/CD68+, e.g., anti-viral cytotoxic T cells in an inflammation reduced environment ( Figure 2 ).

Blood serum from the patient was profiled through comparative proteomics using RayBiotech antibody arrays, as we have published. 8 Heatmapping clearly demonstrated the profound influence of TPE on the circulatory proteome ( Figure 3A ); Venn diagrams, KEGG and biological process databases uncovered 36 proteins that were commonly downregulated between the rounds of TPE, (Figure 3B -D). In agreement with the diminished inflammation and enhanced adaptive immunity that were suggested by Figures 1 and 2 , this longitudinal serum proteomics revealed significant attenuation of inflammatory factors, which was stable and lasted several months ( Figure 3E and F). Regulators of several growth factor pathways that are known to promote tissue repair increased in the systemic milieu: IGF, EGF, TGF-β ( Figure 3E and F). These results establish rapid and significant changes in circulatory proteome of the patient, which are indicative of attenuated inflammation, productive immune response, and enhanced tissue maintenance.

Since the COVID-19 pandemic, roughly 70-80% of patients suffer various sequelae. 11 About 40% of these patients have acute respiratory distress syndrome (ARDS) and one of the main sequelae is pulmonary fibrosis. 12 Although the mechanism of COVID-19-induced ARDS may be different from classical ARDS, the onset and development of pulmonary fibrosis are commonly related to elevated inflammatory cytokines, such as IL-6. 13 Accordingly, antiinflammatory drugs attenuate COVID-19-induced pneumonia. 14, 15 In this study, a patient who was initially healthy, quickly developed health problems after being infected with the novel coronavirus. Moreover, after two months, his health deteriorated to the point of being unable to walk, being physically short of breath, suffering mental fatigue, and diffuse ground-glass appearance was observed throughout his lungs. Clinical and biological analyses strongly suggested systemic inflammation and a lack of productive immune response. After the first TPE treatment, the dyspnea disappeared, and cough subsided. The patient was also able to walk short distances. Interestingly, these changes were observed on day 2 after the first TPE treatment. A month later, the patient was able to walk uphill easily and jog. The decrease in concentration and cognitive fog disappeared, and the patient was able to return to normal life. During the same period, inflammatory macrophage markers robustly diminished and the markers of lymphocytes increased in the blood, suggesting that TPE promoted adaptive immunity and decreased inflammatory response. Such a productive immune response shift became prominent between the second and third rounds of TPE and rounds 1 and 2 were separated by only 5 days, e.g., too quickly for changing leukocyte subset numbers. Longitudinal comparative proteomics demonstrated that many proteins that are associated with inflammaging 16 were attenuated by the Figure 2 . Effect of TPE on lymphoid and myeloid gene expression. A. The expression of T cell, B-cell NK cell markers and IL2 receptor are significantly increased in R2 and R3 compared to R0. CD11b myeloid marker increased in R1 and then returned to R0 levels. CD68the marker of inflammatory myeloid cells, was significantly decreased by the third round of TPE. B. The ratios of lymphoid/CD11b, lymphoid/CD68, CD25/CD11b and CD25/CD68 markers clearly demonstrate the positive effects of TPE in promoting the adaptive rather than the inflammatory immune response. Note the break in Y-axis scale. *P < 0.05, **P < 0.01, ***P < 0.001. rounds of TPE. For instance, pro-inflammatory factors, such as IL-1β, IL-6, and IP-10, stably decreased. In contrast, lipocalin-1 that participates in the sense of taste, and regulators of EGF, IGF, and TGF-β signaling pathways increased, demonstrating a better capacity for tissue maintenance and repair. Of note, the smell/taste reception returned to normal in this patient after TPE. In summary, this case study suggests that TPE may alleviate post COVID-19 sequelae via positive shifts toward adaptive immunity and tissue repair that are concurrent with reduction of inflammation.

The study was approved by the Diagnostics Investigational Review Board (www.dxirb.com) with study identifier -7347. The study was performed under the written informed consent (obtained by Dr. Dobri Kiprov) from the patient for the use and publication of the patient's data. Therapeutic plasma exchange (TPE) was performed as described. 17 Serum, plasma, and PBMC isolation Whole blood was collected immediately before (pre) or after (post) TPE procedure in the clinic and processed into serum, plasma and PBMCs (Histopaque density) as described. 18 Real-time polymerase chain reaction (PCR) Total RNA was extracted from PBMC using the RNeasy mini kit (Qiagen), and the SuperScript III First-Strand Synthesis System (Invitrogen). Real-time PCR was performed on a Bio-Rad iQ5 real-time PCR machine. The primers used for PCR are listed in Table 1 .

Serum was analyzed on a Ray Biotech human L507 antibody capture array (AAH-BLG-1-4, Raybiotech), processed according to the manufacturer's protocol. The array slides were imaged by a Molecular Devices 4000b scanner and data were calculated by Genepix. Normalization was done by bult-in positive and negative controls.

The gene ID of differently regulated proteins was performed using DAVID Bioinformatics Resources (version 6.8, https://david.ncifcrf.gov), as well as the GO (Gene Ontology) analysis of the biological process (BP), molecular function (MF) and cellular component (CC), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway. Heat maps were performed with ClustVis. 19 Volcano plots were constructed with the Graphpad Prism software version 9 (GraphPad software Inc).

All statistical analyses were performed using GraphPad Prism software. All values are expressed as means AE SEM for independent experiments, or SD for replicates. To determine the significance of differences among groups, comparisons were made using Student's t-test. The P < 0.05 was considered significant. The project contains the following underlying data:

[Dataset_1_qPCR raw data.xlsx] (Raw qPCR data).

[Dataset_2_Antibody array raw data.xlsx] (Antibody array raw data).

[Dataset_3_raw data of diagnosis.pdf] (Diagnosis data).

Data are available under the terms of the Creative Commons Attribution 4.0 International license (CC-BY 4.0).

DKiprov planned and performed all clinical work, established the IRB approval, provided Figure 1 and the blood samples to the Conboy laboratory and co-wrote the manuscript; DKim provided Figure 2 , bio-computation and bioinformatics for Figure 3 , and participated in the manuscript writing; ML contributed to Figure 2 ; CL and EW performed the comparative proteomics that is shown in Figure 3 and CL provided the schematic of Figure 1A ; JH, RR and AH provided clinical support; MJK contributed to the planning of this work and co-wrote the manuscript; IC planned, directed, and integrated the study, interpreted the data, and co-wrote the manuscript. All authors agreed with publication of this work.

Is sufficient discussion included of the importance of the findings and their relevance to future understanding of disease processes, diagnosis or treatment? Partly

Is the case presented with sufficient detail to be useful for other practitioners? Yes

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We would like to thank William Hou, Zhixin Zhang and Xiaoyue Mei for formatting the references, and Wu Love for logistics help.

Current Peer Review Status: Version 1 Reviewer Report 25 February 2022 https://doi.org/10.5256/f1000research.78300.r123772 © 2022 Nasa P. This is an open access peer review report distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Department of Critical Care Medicine, NMC Specialty Hospital, Dubai, United Arab Emirates Congratulations authors for the successful outcome of this exploratory study. I have the following points for consideration to make the discussion comprehensive.There is a recent review published in Nature on the pathology of long-haul COVID-19. It will be worth using that in the discussion. (https://doi.org/10.1038/s41590-021-01104-y). The pathophysiology of long-haul COVID-19 involving imbalance between persistent inflammation on homeostasis should be discussed and provide prospects for future controlled studies.

Was plasma removed through therapeutic plasma exchange profiled through comparative proteomics? This would have helped in understanding the degree of reduction of the biomarkers with each session of TPE.

Role of TPE and Plasma exchange has shown variable effects and investigators have used them in different combinations. It is worth including them in discussing ( https://www.ijidonline.com/article/S1201-9712 (20) 32289-X/fulltext) 3.

No competing interests were disclosed. 

Department of Public Health and Clinical Medicine, Umeå University, Umeå, SwedenThe Case Report using Plasmapheresis (apheresis) for long-haul Covid increases awareness of the complexity of the disease and the possibilities to immunomodulate by apheresis.The topic is very important and the concept well described. The case is also well described.There is a lack of information that should be added: What type of apheresis procedure (centrifuge or filtration, leukapheresis?) was used? 1.What type and doses of anticoagulation during apheresis was used? (citrate, LMWH, heparin?)

Was a maintenance pharmacological therapy used also after initiation of apheresis to prohibit antibodies to increase?

If so, what were the pharmacological doses/kg body weight and/day of such medication (or interval)?

What were the time intervals between the apheresis procedures? 5.Did you try to investigate for specific antibodies? 6.You could add the concept of apheresis for antibody removal such as described for VITT by Rock et al. I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

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