Introduction Community-acquired pneumonia has high mortality and is associated with significant healthcare costs. In older adults with community-acquired pneumonia neutrophil dysfunction has been identified and is associated with poor outcomes for patients. Immunometabolism is a rapidly developing field which links immune cell function to metabolism. This study aims to explore neutrophil metabolism in community-acquired pneumonia.
Methods and analysis Pneumonia Metabolism in Ageing study is a prospective observational study recruiting older adults hospitalised with community-acquired pneumonia to examine neutrophil function and metabolic status. Controls will be older adults with no acute illness. The primary endpoint is neutrophil chemotaxis.
Ethics and dissemination The study has ethical approval from the Research Ethics Committee Wales, reference 19/WA/0299. This study involves participants who may lack the capacity to consent to research involvement, in this situation, personal or professional assent will be sought. The results from this study will be submitted for publication in peer-reviewed journals and disseminated at local and international conferences.
- Neutrophil Biology
- Bacterial Infection
- Innate Immunity
- Respiratory Infection
Data availability statement
Data sharing not applicable as no datasets generated and/or analysed for this study.
This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
WHAT IS ALREADY KNOWN ON THIS TOPIC
Neutrophils from older adults with community-acquired pneumonia demonstrate altered effector functions compared with younger adults. However, the mechanism underlying the broad dysfunction seen remains unclear.
WHAT THIS STUDY ADDS
This study investigates neutrophil metabolism, a novel aspect of neutrophil biology in pneumonia and sepsis.
HOW THIS STUDY MIGHT AFFECT RESEARCH, PRACTICE OR POLICY
This study has the potential to lead to a new treatment paradigm in community-acquired pneumonia; targeting the host response alongside antimicrobial therapies.
Community-acquired pneumonia (CAP) is a leading cause of hospitalisation and has high mortality in older adults.1 Mortality is greatest in those with sepsis due to CAP (CAP+S), with survivors experiencing increased mortality for a decade following discharge from hospital.2 The long-term burden of CAP includes cognitive dysfunction, reduced mobility and increased care needs. Readmission following hospitalisation for CAP is common, occurring in 11% of older adults.3
CAP occurs most commonly in adults aged over 65 years, and older adults are more likely to experience severe CAP and CAP+S.4 As the global population is ageing the prevalence of CAP is likely to rise.5
Between 22% and 42% of all CAP episodes require hospitalisation,6 and this places a significant burden on health services. In 2019, hospital treatment for CAP cost the National Health Service £731 million, with costs significantly higher for the treatment of older adults.7
There have been no significant advances in the management of CAP since the advent of antibiotic therapy.
Recovery from CAP requires a functional and coordinated immune response. In CAP, neutrophils are the predominant responding immune cell to infection and the resulting tissue damage. Neutrophils migrate to sites of inflammation and clear infection through bactericidal effector functions including phagocytosis and the generation of neutrophil extracellular traps and reactive oxygen species (RoS).8 These functions can be encompassed by cellular phenotype; the manifestation of cellular processes at gene and protein levels which result in changes in a cell’s function, morphology and surface markers.9
In young adults, CAP is associated with a rapid upregulation of effector functions until the infection is resolved.10 11 However, even in health neutrophil functions in older adults appear depressed,12 this is particularly true in frail older adults13 and data suggest that CAP exacerbates this, with further reductions in neutrophil functions leading to a state of immunoparesis which has been demonstrated for up to 6 weeks following CAP.12 14–16 Differences in neutrophil cellular phenotype have been identified in sepsis17 and disease states such as chronic obstructive pulmonary disease,18 however, there is no literature examining changes in surface marker expression combined with functional assessment in CAP.
This broad impact on effector function suggests that a central cellular mechanism is involved, such as metabolism. Immunometabolism is defined as the role of cellular metabolism in the regulation of immune function19 and there is increasing interest in exploring if therapeutically targeting immunometabolism may optimise immune responses. For example, inhibiting glycolysis in myeloid cells using murine models is associated with an improved recovery from sepsis.20
Neutrophil metabolism is poorly understood, especially in disease states but neutrophils appear to rely on glycolysis for energy generation.21 The effector functions required for a coordinated and effective response to infection are highly energy-demanding processes. Modification of glycolysis in neutrophils may offer a novel therapeutic strategy for CAP. Potential targets include glucose transporters, key enzymes required for glycolysis (hexokinase, phosphofructokinase, pyruvate kinase and lactate dehydrogenase) and lactate transporters/receptors. Evidence to date confirms alterations in these key enzymes during sepsis.22
This manuscript describes a protocol for the assessment of neutrophil function, phenotype and immunometabolism in older adults with CAP, compared with an age, frailty and morbidity-matched cohort in the Pneumonia Metabolism in Ageing (PUMA) study.
Research hypothesis and aims
We hypothesise that depressed neutrophil function seen in older adults with CAP is due to alterations in neutrophil immunometabolism, and that this alteration is modifiable in vitro by modulating glycolysis.
This study aims to functionally phenotype neutrophils from participants with CAP alongside age and frailty-matched cohort while characterising the metabolism of these cells. Figure 1 provides an overview of the study design and outcomes collected. Primary and secondary aims are outlined in table 1.
PUMA is an observational cohort study recruiting adult participants with CAP as defined by the British Thoracic Society.23 This includes symptoms and signs consistent with an acute lower respiratory tract infection associated with radiographic shadowing for which there is no other explanation. Signs and symptoms include three or more of the following: cough, sputum production, breathlessness, pleuritic chest pain, haemoptysis, fever, headache and signs consistent with pneumonia on chest auscultation. Participants with and without sepsis will be recruited. Sepsis is defined as a quick Sequential Organ Failure Assessment score score ≥2.24
The control cohort will be matched as much as possible for age and frailty with no recent acute illness. Matching for frailty will be achieved using clinical frailty scale. Participants will be recruited between March 2020 and November 2024; however, there have been significant periods of disruption relating to the pandemic and other factors. Recruitment is ongoing.
Full inclusion and exclusion criteria for each cohort are in table 2. We have chosen to exclude patients with common conditions or medications known to significantly impact neutrophil function and or metabolism such as chronic obstructive pulmonary disease and haematological malignancy.25 26
The study will be conducted in a single site, at the Queen Elizabeth Hospital, Birmingham, UK (QEHB). The QEHB is a 1200-bed tertiary and acute hospital in an urban area.
Sampling and sample size calculation
CAP cases will be recruited from inpatient wards at QEHB and are expected to remain admitted for ≥24 hours. Controls will be recruited from a range of outpatient clinics at QEHB to enable matching of age, frailty and comorbidity where possible.
The primary outcome measure for sample size calculation is based on a reduction in chemotaxis in patients with CAP compared with age-matched controls. Pilot data indicate a 62% reduction in chemotaxis in CAP cases with SD 0.079 for CAP and 0.135 for controls. To detect a difference in chemotaxis with p<0.005 and 95% power, we will need to recruit eight CAP and eight controls. In the completed SNOOPI study, a 30-day mortality was 16%, and study withdrawal was 6%.11 We estimate we need to recruit two CAP participants to account for drop-outs. Total sample size: 10 CAP and 8 controls. This limited sample size is not anticipated to inform relationships between clinical outcomes and neutrophil function but is powered to detect a biological endpoint (difference in neutrophil chemotaxis between CAP and controls).
Study visit procedure
Participant identification, consent and follow-up
Where possible CAP participants will be recruited within 36 hours of hospital admission, then follow-up visits between day three and five (if remaining an inpatient) and then 6–8 weeks following admission, where possible the 6–8 weeks visit will be timed to coincide with follow-up chest radiograph when requested by the clinical team. Drop-outs to follow-up are expected due to death, discharge prior to days 3–5, withdrawal and unwillingness to return to hospital for 6–8 weeks visit. Study procedures are shown in figure 2. CAP frequently causes delirium, and dementia is a common comorbidity of older adults with CAP, therefore, CAP participants who lack the ability to consent to enrolment are not excluded. In the case of impaired capacity to consent to study enrolment a personal consultee opinion will be sought in the first instance, if no personal consultee is available an independent professional consultee’s opinion will be sought. Retrospective consent will be sought in these cases.
Control participants will be recruited at a single time point only.
At each study visit participants will undergo a detailed clinical history to ascertain factors which may influence neutrophil function, and outcome of CAP, as described in figure 3. We will also record information related to the hospital admission such as treatment strategies that may influence outcomes. Traditionally studies of CAP have considered binary outcomes such as survived/died, however, our public and patient involvement and engagement work demonstrated that a more nuanced approach was preferred. Therefore, we will collect information on postdischarge mobility, care needs and readmissions to hospital. Due to the limited size of the planned study, the comparisons using this data are intended to be exploratory and ensure the CAP and control cohorts are well matched.
For CAP participants, blood samples for research will be taken alongside clinically indicated blood samples to reduce number of venepuncture episodes for both CAP and control participants. Maximum of 45 mL blood will be taken at each study visit for research purposes.
Blood samples will predominantly be used in neutrophil isolation, processing and downstream use is described in table 3.
Neutrophil isolation and functional assays
Isolated neutrophils will be prepared by discontinuous Percoll density centrifugation.18 Briefly, whole blood is gently mixed with 2% dextran in 6:1 ratio to enable sedimentation of red blood cells. Discontinuous Percoll solutions are prepared by diluting in either 1.54M NaCl or 0.154M NaCl to generate 90% and 56% solutions, respectively. The buffy coat is then layered over the discontinuous Percoll solution. The gradient is centrifuged at 470 g for 20 min at room temperature with no break or acceleration. The neutrophil layer is harvested and washed in phosphate buffered saline (PBS) to form a pellet. The neutrophils are resuspended in RPMI 1640 for downstream use. Neutrophils are typically >97% pure and >95% viable as assessed annexin/propidium iodide staining. Due to limitations in cell number, not all experimental assays will be carried out for each participant.
Neutrophil chemotaxis is assessed to a chemoattractant (interlukin-8) using a modified Insall chamber as described in.26 Use of the Insall chamber with time lapse filming using video microscopy allows for quantification of speed and directionality of individual neutrophils. To analyse the time lapse filming 10 neutrophils are selected at random and their movement tracked using FIJI Image J. These tracking data are then used to calculate speed, velocity, persistence and overall accuracy. Neutrophils migrate using proteinases to navigate extracellular matrices; therefore, speed and accuracy are important in assessing migratory parameters.26
Neutrophil lysates are prepared for RNA extraction and protein lysate for Western blotting and stored at −80°C. RNA will be used in RNA sequencing, targets identified involved in metabolism will be confirmed at the protein level.
Neutrophil oxidative burst is assessed using the Seahorse Analyzer (Agilent Technologies). In brief, neutrophils are treated with inhibitors of mitochondrial respiration (rotenone/anti-mycin A) followed by phorbol 12-myristate 13-acetate (PMA) treatment to generate RoS.27 Oxygen consumption is then measured to assess oxidative burst from the neutrophils over a time course. This method allows comparison of overall oxygen uptake and time taken to reach maximal oxygen uptake.
Neutrophil cell surface marker expression
Neutrophil phenotype will be assessed by staining isolated neutrophils with antibodies that bind to extracellular surface markers. Antibodies to detect cluster of differentiation (CD) 11b, CD66b, CD10, CXC chemokine receptor (CXCR) 2 and CXCR4 are mixed as one cocktail, while antibodies that bind CD16, CD11c, CD62L, CD54 and programmed death-ligand (PD-L) 1 are mixed as a second cocktail. The antibody cocktails as well as isotype controls are added to neutrophils and incubated on ice for 30 min in the dark. Unstained controls are also included in the incubation. After incubation, neutrophils are washed with 1% bovine serum albumin in PBS (FACS buffer) and centrifuged at 300 g for 5 min. The neutrophils are resuspended in FACS buffer and analysed using a MACSQuant 10 flow cytometer (Miltenyl Biotec). Data are analysed using FlowJo software. The analysis of the expression of surface receptors will allow for comparison of neutrophil phenotype in terms of their activation, maturity, senescence, reverse migration, respiratory burst and immunosuppression.
Neutrophil metabolism will be assessed using the Seahorse Analyzer (Agilent Technologies) to measure extracelllar acidification rate (ECAR) of media as a surrogate of lactate efflux.27 The assay involves use of both glycolytic and mitochondrial inhibitors to interrogate metabolic pathways. Freshly isolated neutrophils are seeded on a cell plate, ECAR is measured over time with injection of PMA (a potent stimulator of neutrophils) after measurement of baseline glycolysis, a subsequent injection of oligomycin inhibits mitochondrial activity to confirm that all measured activity is glycolytic in origin. Lastly, 2-deoxyglucose, an inhibitor of glycolysis, is added to confirm all metabolic activity is shutdown. Baseline glycolysis, maximal glycolysis and induced glycolysis can be measured using this assay.
Transcriptomic analysis will be carried out in collaboration with Genomics department at University of Birmingham. Total RNA will be extracted using the RNAqueous Micro Total RNA Isolation Kit (to include an on-column DNase treatment). RNA quality will be measured using the Agilent 2200 Tapestation. The polyA+mRNA fractionation will be isolated and cDNA libraries prepared using the QuantSeq 3‘mRNA-Seq Library Prep Kit. Samples will then be subjected to 75 bp, single-end sequencing using Illumina 2500 sequencing machine. Paired end reads will be aligned to the human reference genome (hg38) using STAR and differential gene expression will be determined using DESeq2.
Public and patient involvement and engagement
Patient involvement led to the following changes in the research protocol; where possible the 6-week follow-up visit would occur either as a home visit, or when the participant returned to the hospital for follow-up chest radiographs as commonly occurs following treatment for CAP. In addition, following discussion with patients we expanded information collected on follow-up to include care needs, readmission and mobility changes. Finally, we included a follow-up letter at the end of the study to all participants to thank them for their involvement and update them on the study’s findings. All study documents have been reviewed by patient representatives.
Data will be analysed using SPSS for Windows V.26.0, GraphPad Prism V.9.0 or R V.4.2 or later. For continuously distributed data, differences between groups will be tested using independent sample t-tests with transformations of variables to normality if appropriate or non-parametric equivalents. χ2 tests (or Fisher’s exact tests) will be used for categorical variables. Any comparisons of clinical parameters such as impact of CAP severity will be considered exploratory.
The results of this study will be submitted to peer-reviewed journals for publication and will be presented at local and national conferences. We will adhere to Enhancing the QUAlity and Transparency Of health Research (EQUATOR) guidelines for observational studies and follow International Committee of Medical Journal Editors (ICMJE) best practice in generation of the study manuscript. No participants will be identified in publications that result from this study.
Local monitoring of the study will include the following: confirmation of informed consent or assent, source data verification, backup and validation of data input. A random sample (10%) of case report forms will be checked to ensure accurate data input.
We do not anticipate any safety concerns during this study. Any adverse events will be immediately reported to the chief investigator, and they will assess causality and seriousness.
Data availability statement
Data sharing not applicable as no datasets generated and/or analysed for this study.
Patient consent for publication
This study involves human participants and this study has received favourable ethical approval from Research Ethics Committee (Wales), reference 19/WA/0299. Participants gave informed consent to participate in the study before taking part.
Contributors FSG participated in designing and planning all parts of the study and drafting the manuscript. AAF, AS, ES and DRT participated in conception and designing and planning all parts of the study and conducted a critical review of the manuscript.
Funding This work was supported by the following: Dunhill Medical Trust grant number RTF1906\86. Health Data Research-UK (NIHR129593), Asthma+Lung UK (MCFPHD20F\2). Efficacy and Mechanism Evaluation (NIHR131600), Health Technology Assessment (NIHR129593) and Medical Research Council (MR/S002782/1).
Competing interests None declared.
Patient and public involvement Patients and/or the public were involved in the design, or conduct, or reporting, or dissemination plans of this research. Refer to the Methods section for further details.
Provenance and peer review Not commissioned; externally peer reviewed.