Rachel Tanner

Rachel Tanner
  • BA Hons, MA, DPhil Clinical Medicine, AFHEA
  • Professor (Associate) at University of Oxford

About

120
Publications
20,929
Reads
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11,154
Citations
Current institution
University of Oxford
Current position
  • Professor (Associate)
Additional affiliations
January 2021 - January 2024
Wolfson College, University of Oxford
Position
  • Research Associate
October 2017 - September 2019
Somerville College, University of Oxford
Position
  • Fellow
September 2017 - present
Wadham College, University of Oxford
Position
  • Lecturer
Education
October 2012 - October 2015
University of Oxford
Field of study
  • Clinical Medicine
October 2003 - June 2007
University of Oxford
Field of study
  • Biological Sciences

Publications

Publications (120)
Article
Full-text available
The current vaccine against tuberculosis, live attenuated Mycobacterium bovis BCG, has variable efficacy, but development of an effective alternative is severely hampered by the lack of an immune correlate of protection. There has been a recent resurgence of interest in functional in vitro mycobacterial growth inhibition assays (MGIAs), which provi...
Article
Full-text available
Tuberculosis (TB) remains a serious global health threat and an improved vaccine is urgently needed. New candidate TB vaccines are tested using preclinical animal models such as mice, guinea pigs, cattle and non-human primates. Animals are routinely infected with virulent Mycobacterium tuberculosis (M.tb) in challenge experiments to evaluate protec...
Article
Full-text available
Tuberculosis (TB) continues to pose a serious global health threat, and the current vaccine, BCG, has variable efficacy. However, the development of a more effective vaccine is severely hampered by the lack of an immune correlate of protection. Candidate vaccines are currently evaluated using preclinical animal models, but experiments are long and...
Article
Full-text available
Background There is an urgent need for improved vaccines to protect against tuberculosis. The currently available vaccine Bacille Calmette-Guerin (BCG) has varying immunogenicity and efficacy across different populations for reasons not clearly understood. MVA85A is a modified vaccinia virus expressing antigen 85A from Mycobacterium tuberculosis wh...
Article
Full-text available
The only currently licensed vaccine against tuberculosis (TB), Bacille Calmette Guérin (BCG), is insufficient to control the epidemic. MTBVAC is a live attenuated strain of Mycobacterium tuberculosis (M.tb) and is one the most advanced TB vaccine candidates in the pipeline. It is more efficacious than BCG in preclinical models including non-human p...
Article
Full-text available
A new and more effective tuberculosis (TB) vaccine is urgently needed, but development is hampered by the lack of validated immune correlates of protection. Bacillus Calmette Guérin (BCG) vaccination by the aerosol (AE) and intravenous (IV) routes has been shown to confer superior levels of protection from challenge with Myco-bacterium tuberculosis...
Article
Full-text available
Introduction Mycobacteria are known to exert a range of heterologous effects on the immune system. The mycobacteria-based Freund’s Complete Adjuvant is a potent non-specific stimulator of the immune response used in immunization protocols promoting antibody production, and Mycobacterium bovis Bacille Calmette Guérin (BCG) vaccination has been linke...
Article
Background A SARS-CoV-2 controlled human infection model (CHIM) has been successfully established in seronegative individuals using a dose of 1×10¹ 50% tissue culture infectious dose (TCID50) pre-alpha SARS-CoV-2 virus. Given the increasing prevalence of seropositivity to SARS-CoV-2, a CHIM that could be used for vaccine development will need to in...
Article
Full-text available
Introduction First described by Wallis et al. in 2001 for the assessment of TB drugs, the direct mycobacterial growth inhibition assay (MGIA) offers a tractable ex vivo tool measuring the combined influences of host immunity, strain virulence and intervention effects. Over the past 13 years, we have led efforts to adapt the direct MGIA for the asse...
Conference Paper
Introduction Controlled human infection models (CHIMs) involve the deliberate exposure of individuals to a pathogen in a controlled environment. Respiratory organism CHIMs have been utilised to further understanding on the kinetics of infection or host-pathogen immunobiology plus enabling expedited testing of vaccines and therapeutics. A SARS-CoV-2...
Article
Full-text available
Tuberculosis vaccine development is hindered by the lack of validated immune correlates of protection. Exploring immune correlates of risk of disease and/or infection in prospective samples can inform this field. We investigate whether previously identified immune correlates of risk of TB disease also associate with increased risk of M.tb infection...
Article
Full-text available
Abstract Background Despite widespread searches, there are currently no validated biofluid markers for the detection of subclinical neuroinflammation in multiple sclerosis (MS). The dynamic nature of human metabolism in response to changes in homeostasis, as measured by metabolomics, may allow early identification of clinically silent neuroinflamma...
Article
Full-text available
Vaccination, as a public health measure, offers effective protection of populations against infectious diseases. Optimising vaccination efficacy, particularly for higher-risk individuals, like the elderly whose immunocompromised state can prevent the development of robust vaccine responses, is vital. It is now clear that 24-hour circadian rhythms,...
Article
Full-text available
Bacille Calmette-Guérin (BCG), the only currently licenced tuberculosis vaccine, may exert beneficial non-specific effects (NSE) in reducing infant mortality. We conducted a randomised controlled clinical study in healthy UK adults to evaluate potential NSE using functional in-vitro growth inhibition assays (GIAs) as a surrogate of protection from...
Preprint
Full-text available
Tuberculosis vaccine development is hindered by the lack of validated immune correlates of protection. Exploring immune correlates of risk of disease and/or infection in prospective samples can inform this field. We investigated whether previously identified immune correlates of risk of TB disease also associate with increased risk of M.tb infectio...
Article
Full-text available
Tuberculosis (TB) is a major global health problem and the only currently-licensed vaccine, BCG, is inadequate. Many TB vaccine candidates are designed to be given as a boost to BCG; an understanding of the BCG-induced immune response is therefore critical, and the opportunity to relate this to circumstances where BCG does confer protection may dir...
Article
Full-text available
We present a non-human primate mycobacterial growth inhibition assay (MGIA) using in vitro blood or cell co-culture with the aim of refining and expediting early tuberculosis vaccine testing. We have taken steps to optimise the assay using cryopreserved peripheral blood mononuclear cells, transfer it to end-user institutes, and assess technical and...
Article
Full-text available
The only currently available approach to early efficacy testing of tuberculosis (TB) vaccine candidates is in vivo preclinical challenge models. These typically include mice, guinea pigs and non-human primates (NHPs), which must be exposed to virulent M.tb in a ‘challenge’ experiment following vaccination in order to evaluate protective efficacy. T...
Article
Although only a small fraction will ever develop the active form of tuberculosis (ATB) disease, chemoprophylaxis treatment in latent TB infected (LTBI) individuals is an effective strategy to control pathogen transmission. Characterizing immune responses in LTBI upon chemoprophylactic treatment is important to facilitate treatment monitoring, and t...
Article
Full-text available
2021 is the 100-year anniversary of the BCG vaccine, and there is a lot to celebrate! This vaccine has without doubt saved the lives of millions of people, by protecting them from the bacterial lung disease tuberculosis (TB) and possibly other illnesses too. However, there are some drawbacks to BCG—in particular, it does not work very well in some...
Article
Full-text available
This study describes the use of cynomolgus macaques of Chinese origin (CCM) to evaluate the efficacy and immunogenicity of the BCG vaccine against high dose aerosol Mycobacterium tuberculosis challenge. Progressive disease developed in three of the unvaccinated animals within 10 weeks of challenge, whereas all six vaccinated animals controlled dise...
Article
Full-text available
p>More than 190 vaccines are currently in development to prevent infection by the novel severe acute respiratory syndrome coronavirus 2. Animal studies suggest that while neutralizing antibodies against the viral spike protein may correlate with protection, additional antibody functions may also be important in preventing infection. Previously, we...
Article
Full-text available
This review critically assesses the body of research about Measles-Mumps-and-Rubella (MMR) vaccine attitudes and uptake in the United Kingdom (UK) over the past 10 years. We searched PubMed and Scopus, with terms aimed at capturing relevant literature on attitudes about, and uptake of, the MMR vaccine. Two researchers screened for abstract eligibil...
Preprint
This review critically assesses the body of research about Measles-Mumps-and-Rubella (MMR) vaccine attitudes and uptake in the United Kingdom (UK) over the past 10 years. We searched PubMed and Scopus, with terms aimed at capturing relevant literature on attitudes, uptake, decision-making, and beliefs about the MMR vaccine. Two researchers screened...
Article
Full-text available
The only currently available approach to early efficacy testing of tuberculosis (TB) vaccine candidates is in vivo preclinical challenge models. These typically include mice, guinea pigs and non-human primates (NHPs), which must be exposed to virulent M.tb in a ‘challenge’ experiment following vaccination in order to evaluate protective efficacy. T...
Article
Full-text available
Background The ChAdOx1 nCoV-19 (AZD1222) vaccine has been approved for emergency use by the UK regulatory authority, Medicines and Healthcare products Regulatory Agency, with a regimen of two standard doses given with an interval of 4–12 weeks. The planned roll-out in the UK will involve vaccinating people in high-risk categories with their first d...
Preprint
Full-text available
This study describes the use of cynomolgus macaques of Chinese origin (CCM) to evaluate the efficacy and immunogenicity of the BCG vaccine against high dose aerosol Mycobacterium tuberculosis challenge. Progressive disease developed in three of the unvaccinated animals within ten weeks of challenge, whereas all six vaccinated animals controlled dis...
Preprint
Full-text available
Many tuberculosis (TB) vaccine candidates are designed as a boost to BCG; an understanding of the BCG-induced immune response is therefore critical, and the opportunity to relate this to circumstances where BCG does protect may direct the design of more efficacious vaccines. While the T cell response to BCG vaccination has been well-characterised,...
Preprint
Full-text available
Tuberculosis (TB) vaccine candidates must be tested for safety and efficacy using preclinical challenge models prior to advancement to human trials, because of the lack of a validated immune correlate or biomarker of protection. New, unbiased tools are urgently needed to expedite the selection of vaccine candidates at an early stage of development...
Article
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of Coronavirus Disease 2019 (COVID-19), has caused a global pandemic, and safe, effective vaccines are urgently needed1. Strong, Th1-skewed T cell responses can drive protective humoral and cell-mediated immune responses2 and might reduce the potential for disease enh...
Article
Full-text available
Background A safe and efficacious vaccine against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), if deployed with high coverage, could contribute to the control of the COVID-19 pandemic. We evaluated the safety and efficacy of the ChAdOx1 nCoV-19 vaccine in a pooled interim analysis of four trials. Methods This analysis includes dat...
Article
Older adults are at higher risk of severe disease and death if they develop COVID-19 and are therefore a priority for immunisation should an efficacious vaccine be developed. Immunogenicity of vaccines is often poorer in older adults as a result of immunosenescence. We recently reported the immunogenicity of a novel viral vectored vaccine, ChAdOx1...
Article
Full-text available
Background Older adults (aged ≥70 years) are at increased risk of severe disease and death if they develop COVID-19 and are therefore a priority for immunisation should an efficacious vaccine be developed. Immunogenicity of vaccines is often worse in older adults as a result of immunosenescence. We have reported the immunogenicity of a novel chimpa...
Article
Full-text available
Background The pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) might be curtailed by vaccination. We assessed the safety, reactogenicity, and immunogenicity of a viral vectored coronavirus vaccine that expresses the spike protein of SARS-CoV-2. Methods We did a phase 1/2, single-blind, randomised controlled trial in five t...
Article
Full-text available
In the absence of a correlate(s) of protection against human tuberculosis and a validated animal model of the disease, tools to facilitate vaccine development must be identified. We present an optimised ex vivo mycobacterial growth inhibition assay (MGIA) to assess the ability of host cells within the lung to inhibit mycobacterial growth, including...
Article
Full-text available
Tuberculosis (TB) remains a leading global cause of morbidity and mortality and an effective new vaccine is urgently needed. A major barrier to the rational development of novel TB vaccines is the lack of a validated immune correlate or biomarker of protection. Mycobacterial Growth Inhibition Assays (MGIAs) provide an unbiased measure of ability to...
Article
Full-text available
Immune activation is associated with increased risk of tuberculosis (TB) disease in infants. We performed a case control analysis to identify drivers of immune activation and disease risk. Among 49 infants who developed TB disease over the first two years of life, and 129 matched controls who remained healthy, we found the cytomegalovirus (CMV) sti...
Article
Full-text available
Bacillus Calmette Guérin (BCG) is the only currently available vaccine against tuberculosis (TB), but it confers incomplete and variable protection against pulmonary TB in humans and bovine TB (bTB) in cattle. Insights into the immune response induced by BCG offer an underexploited opportunity to gain knowledge that may inform the design of a more...
Article
Full-text available
A major challenge to tuberculosis (TB) vaccine development is the lack of a validated immune correlate of protection. Mycobacterial growth inhibition assays (MGIAs) represent an unbiased measure of the ability to control mycobacterial growth in vitro. A successful MGIA could be applied to preclinical and clinical post-vaccination samples to aid in...
Article
Full-text available
A correction has been published and is appended to both the HTML and PDF versions of this paper. The error has not been fixed in the paper.
Article
Full-text available
Inducible nitric oxide synthase (iNOS) plays a crucial role in controlling growth of Mycobacterium tuberculosis (M.tb), presumably via nitric oxide (NO) mediated killing. Here we show that leukocyte-specific deficiency of NO production, through targeted loss of the iNOS cofactor tetrahydrobiopterin (BH4), results in enhanced control of M.tb infecti...
Article
Full-text available
Soil-transmitted helminths and Mycobacterium tuberculosis frequently coincide geographically and it is hypothesized that gastrointestinal helminth infection may exacerbate tuberculosis (TB) disease by suppression of Th1 and Th17 responses. However, few studies have focused on latent TB infection (LTBI), which predominates globally. We performed a l...
Article
Full-text available
A major contribution to the burden of Tuberculosis (TB) comes from latent Mycobacterium tuberculosis infections (LTBI) becoming clinically active. TB and LTBI probably exist as a spectrum and currently there are no correlates available to identify individuals with LTBI most at risk of developing active disease. We set out to identify immune paramet...
Article
Full-text available
The similarities between certain animals and humans mean that animal research can be very useful in understanding how the human body works and in developing and testing new medicines. Many major medical breakthroughs have been made with the help of animal experiments, including the invention of antibiotics, vaccines, and cancer treatments. However,...
Article
Full-text available
Migrants and ethnic minorities in the UK have higher rates of tuberculosis (TB) compared with the general population. Historically, much of the disparity in incidence between UK-born and migrant populations has been attributed to differential pathogen exposure, due to migration from high-incidence regions and the transnational connections maintaine...
Article
Full-text available
The 5th Global Forum on TB Vaccines was held in New Delhi, India from 20 to 23 February 2018. This was the largest Global Forum on TB Vaccines to date with nearly 350 participants from more than 30 countries. The program included over 60 speakers in 12 special, plenary and breakout sessions and 72 posters. This Global Forum brought a great sense of...
Article
Full-text available
Migrants and ethnic minorities in the UK have higher rates of tuberculosis (TB) compared with the general population. Historically, much of the disparity in incidence between UK-born and migrant populations has been attributed to differential pathogen exposure, due to migration from high-incidence regions and the transnational connections maintaine...
Article
Full-text available
Immune activation is associated with increased risk of tuberculosis (TB) disease in infants. We performed a case control analysis to identify drivers of immune activation and disease risk. Among 49 infants who developed TB disease over the first two years of life, and 129 matched controls who remained healthy, we found the cytomegalovirus (CMV) sti...
Article
Full-text available
The lack of validated immunological correlates of protection makes tuberculosis vaccine development difficult and expensive. Using intradermal bacille Calmette-Guréin (BCG) as a surrogate for aerosol Mycobacterium tuberculosis (M.tb) in a controlled human infection model could facilitate vaccine development, but such a model requires preclinical va...
Article
Full-text available
The development of a functional biomarker assay in the tuberculosis (TB) field would be widely recognized as a major advance in efforts to efficiently develop and test novel TB vaccine candidates. We present preliminary studies using mycobacterial growth inhibition assays (MGIAs) to detect a BCG vaccine response across species, and extend this work...
Article
Human tuberculosis remains a significant cause of mortality and morbidity throughout the world. The global economic impact of bovine TB is considerable. An effective vaccine would be the most cost-effective way to control both epidemics, particularly in emerging economies. TB vaccine research would benefit from the identification of an immune corre...
Article
Full-text available
Background In the absence of a validated animal model and/or an immune correlate which predict vaccine-mediated protection, large-scale clinical trials are currently the only option to prove efficacy of new tuberculosis candidate vaccines. Tools to facilitate testing of new tuberculosis (TB) vaccines are therefore urgently needed. Methods We presen...
Article
Full-text available
Nature Communications 7, Article number: 11290 10.1038/ncomms11290 (2016); Published: April122016; Updated: May062016 The original version of this Article contained an error in the spelling of the author Mark Hatherill, which was incorrectly given as Mark Hatheril. This has now been corrected in both the PDF and HTML versions of the Article.
Article
Vaccines to protect against tuberculosis (TB) are urgently needed. We performed a case-control analysis to identify immune correlates of TB disease risk in Bacille Calmette-Guerin (BCG) immunized infants from the MVA85A efficacy trial. Among 53 TB case infants and 205 matched controls, the frequency of activated HLA-DR(+) CD4(+) T cells associates...
Article
Full-text available
Background: The relevance of antibodies (Abs) in the defense againstMycobacterium tuberculosisinfection remains uncertain. We investigated the role of Abs to the mycobacterial capsular polysaccharide arabinomannan (AM) and its oligosaccharide fragments in humans. Methods: Sera from 29 healthy adults before and after primary or secondary BCG vacc...
Article
Full-text available
The ratio of monocytes and lymphocytes (ML ratio) in peripheral blood is associated with tuberculosis and malaria disease risk and cancer and cardiovascular disease outcomes. We studied anti-mycobacterial function and the transcriptome of monocytes in relation to the ML ratio. Mycobacterial growth inhibition assays of whole or sorted blood were per...
Article
Full-text available
The testing of vaccines for tuberculosis is costly and time-consuming, and dependent on preclinical animal challenge models and clinical trials. We have recently developed a mycobacterial growth inhibition assay (MGIA) to test vaccine efficacy ex vivo. This assay measures the summative effect of the host immune response and may serve as a novel too...
Conference Paper
The mechanisms of immune protection from Mycobacterium tuberculosis have not been fully elucidated. There is much interest in identifying a valid correlate or biomarker of protection for the down-selection of new TB vaccine candidates. To date, we have used a Bactec MGIT-based in vitro assay to demonstrate a BCG vaccine-induced effect in humans, no...
Article
Full-text available
Background: Tuberculosis (TB) remains a global health problem, with vaccination likely to be a necessary part of a successful control strategy. Results of the first Phase 2b efficacy trial of a candidate vaccine, MVA85A, evaluated in BCG-vaccinated infants were published last year. Although no improvement in efficacy above BCG alone was seen, cryo...
Article
Full-text available
The first phase IIb safety and efficacy trial of a new tuberculosis vaccine since BCG was completed in October 2012. BCG-vaccinated South African infants were randomised to receive Modified Vaccinia virus Ankara, expressing the Mycobacterium tuberculosis antigen 85A (MVA85A), or placebo. MVA85A did not significantly boost the protective effect of B...
Article
Full-text available
Background. A new vaccine is urgently needed to combat tuberculosis. However, without a correlate of protection, selection of the vaccines to take forward into large-scale efficacy trials is difficult. Use of bacille Calmette-Guérin (BCG) as a surrogate for human Mycobacterium tuberculosis challenge is a novel model that could aid selection. Method...
Article
Despite the widespread use of the BCG vaccine there are more than 9 million new cases of tuberculosis (TB) every year and there is an urgent need for better TB vaccines. TB vaccine candidates are selected for evaluation based in part on the detection of an antigen-specific IFN-γ response. The measurement of mycobacterial growth in blood specimens o...
Article
Full-text available
Development of an improved vaccine against tuberculosis (TB) is hindered by the lack of a surrogate of protection. Efficacy of new TB vaccines in humans can only be evaluated by expensive and time consuming efficacy trials within TB endemic areas. It is critical that vaccines with the greatest potential to protect are selected for these trials. Myc...
Conference Paper
Introduction TB vaccine studies to date have used IFN-γ as the main immunological read-out, but this may not be reliable. There is much interest in emerging functional assays which take into account a whole range of cellular mechanisms, such as in vitro Mycobacterial Growth Inhibition Assays (MGIAs). Such an assay would allow down-selection or ‘gat...
Article
Background: New vaccines to prevent tuberculosis are urgently needed. MVA85A is a novel viral vector TB vaccine candidate designed to boost BCG-induced immunity when delivered intradermally. To date, intramuscular delivery has not been evaluated. Skin and muscle have distinct anatomical and immunological properties which could impact upon vaccine-...
Article
Full-text available
HIV-1 accumulates mutations in and around reactive epitopes to escape recognition and killing by CD8+ T cells. Measurements of HIV-1 time to escape should therefore provide information on which parameters are most important for T cell-mediated in vivo control of HIV-1. Primary HIV-1-specific T cell responses were fully mapped in 17 individuals, and...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP45 Sample timepoint :: w02 Days post-screening :: 0...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP210 Sample timepoint :: w22 Days post-screening :: 1...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP210 Sample timepoint :: w22 Days post-screening :: 1...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP45 Sample timepoint :: w02 Days post-screening :: 0...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP210 Sample timepoint :: w22 Days post-screening :: 1...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP210 Sample timepoint :: w22 Days post-screening :: 1...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP210 Sample timepoint :: w22 Days post-screening :: 1...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP45 Sample timepoint :: w02 Days post-screening :: 0...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP45 Sample timepoint :: w02 Days post-screening :: 0...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP210 Sample timepoint :: w12 Days post-screening :: 7...
Data
Annotation information was provided by the author. Some of the information does not have GenBank feature identifiers and is being provided in the comment section. Information in this section is searchable in HIV-1 Database at Los Alamos (hiv.lanl.gov). ##HIVDataBaseData-START## Patient code :: CAP45 Sample timepoint :: w52 Days post-screening :: 35...

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