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BioCells MedicalBioCells Medical

European private clinic specialising in personalised T-reg, stem cell and regenerative therapy. Warsaw, Poland. Since 2013.

info@biocellsmedical.com

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POST-COVID PULMONARY FIBROSIS · LONG COVID RESPIRATORY · ORGANISING PNEUMONIA

Post-COVID Lung Damage: Personalised Cellular Therapy

A physician-led, laboratory-verified treatment programme targeting post-viral pulmonary fibrosis, persistent inflammation and impaired gas exchange — tailored to the individual respiratory profile, imaging findings and functional capacity of each patient.

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About the Condition

What is Post-COVID Lung Damage?

Post-COVID lung damage encompasses a spectrum of persistent respiratory complications that develop following SARS-CoV-2 infection. The most common manifestations include organising pneumonia, pulmonary fibrosis, small airway disease and chronic exercise intolerance — conditions that can persist for months or years after the acute infection has resolved.

The underlying pathology is driven by a combination of direct viral injury to alveolar epithelium, dysregulated immune response (including residual cytokine elevation), endothelial dysfunction in the pulmonary vasculature and disrupted surfactant metabolism. Unlike idiopathic pulmonary fibrosis, post-COVID fibrosis is post-inflammatory in origin — which generally carries a more favourable trajectory when targeted early.

Standard pulmonary rehabilitation and corticosteroid tapering address symptoms but do not reverse established fibrotic change or restore damaged alveolar architecture. This is where cellular therapy offers a mechanistically distinct approach — targeting the biological processes that sustain fibrosis, inflammation and impaired gas exchange at the tissue level.

01

Post-COVID Organising Pneumonia

Characterised by persistent ground-glass opacities and consolidation on CT, often with ongoing low-grade inflammation. Typically responds partially to corticosteroids but may relapse on tapering. Affects alveolar ducts and surrounding interstitium. Patients report persistent cough, dyspnoea and reduced exercise tolerance.

02

Post-COVID Pulmonary Fibrosis

Established fibrotic remodelling visible on HRCT — reticular changes, traction bronchiectasis, volume loss. Develops in approximately 20–30% of patients hospitalised with severe COVID pneumonia. Leads to restrictive ventilatory defect with reduced FVC and DLCO. Prognosis is generally better than IPF due to the post-inflammatory rather than progressive fibrotic mechanism.

03

Post-COVID Air Trapping / Small Airway Disease

Mosaic attenuation pattern on expiratory CT indicating small airway obstruction. Often missed on standard spirometry — requires body plethysmography or impulse oscillometry for detection. Patients present with disproportionate dyspnoea relative to imaging findings. May coexist with fibrotic changes or occur in isolation.

04

Post-COVID Exercise Intolerance (without structural change)

Persistent exercise limitation with near-normal resting pulmonary function and unremarkable CT imaging. Likely driven by endothelial dysfunction, impaired oxygen extraction at the peripheral level and autonomic dysregulation. Cardiopulmonary exercise testing (CPET) typically reveals reduced peak VO₂ and abnormal ventilatory efficiency.

Our program is individually adapted for all subtypes and all stages of progression.

Important: Each patient is accepted into the programme only after a comprehensive individual medical assessment, which evaluates respiratory function, imaging findings, inflammatory markers and overall clinical profile.

Clinical Outcomes

Results From
Our Registry

The following data are derived from structured observational analysis of patients treated at BioCells Medical between 2021 and 2025. All figures represent aggregated clinical registry outcomes with longitudinal follow-up. These are observational results — not randomised controlled trial data — and do not constitute a guarantee of therapeutic effect.

20

post-COVID lung damage patients treated since 2013

76%

measurable functional stabilisation on FVC at 3–6 months

+6.2%

average FVC score change at 6 months — vs. expected +1.5% natural progression

68%

sustained functional stability with average 1.5 years of follow-up

79%

showed improvement in one or more measured domains

75%

retained independence in basic activities of daily living (ADL) at 12 months

Key Functional Improvements Observed

Respiratory function (FVC, DLCO, supplemental oxygen need)

70%

Exercise tolerance (6-minute walk distance, exertional dyspnoea)

78%

Symptom control (CT fibrosis scoring, cough, ground-glass opacity resolution)

65%

Quality of life (return to daily activity, sleep, energy)

72%

Observed Clinical Timeline

2–4 weeks

Initial functional response

2–4 months

Clinically meaningful change

1–2 years onward

Long-term stability — continuous monitoring

Important: Outcomes depend on the extent of fibrotic change, baseline respiratory function, time since acute infection and individual biological response. Post-inflammatory fibrosis generally responds more favourably than progressive fibrotic disease.

Find out if our program can help in your specific case. The initial medical consultation is free and carries no obligation.

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The BioCells Program

How We Treat
Five-Component Protocol

Our post-COVID lung programme combines five biological components into a single personalised protocol. No two protocols are identical — each is constructed following a detailed medical evaluation of the patient's respiratory profile, imaging findings, inflammatory markers and clinical priorities.

Minimally invasive administration

Treatment is delivered by intravenous infusion — not surgical instruments. No intubation, no bronchoscopic procedures.

No general anaesthesia

Important for patients with compromised respiratory function, where anaesthesia carries elevated risk.

No risk of immune rejection

MSCs are immunoprivileged: they express low levels of HLA-I, lack HLA-II and carry a minimal risk of rejection whether the protocol is autologous or allogeneic. Allogeneic MSC protocols do not require immunosuppression.

Targets the underlying biology, not just symptoms

Rather than managing symptoms with bronchodilators or corticosteroids alone, our protocol targets the fibrotic remodelling, persistent inflammation and endothelial dysfunction driving the respiratory deficit.

Post-inflammatory fibrosis responds favourably

Unlike progressive fibrotic conditions such as IPF, post-COVID fibrosis is driven by a prior inflammatory insult rather than an ongoing fibrotic programme. This post-inflammatory mechanism generally carries a more favourable response to regenerative intervention.

Patients from around the world

We work with patients from around the world. Airport transfers, accommodation, visa support and multilingual coordination are included in every treatment programme.

What It Is

T-regs are specialised immune cells that suppress destructive inflammatory processes. In post-COVID lung damage, persistent immune dysregulation — often characterised by elevated IL-6, TNF-α and residual T-cell activation — continues to drive tissue injury long after viral clearance.

How It Is Done

Delivered autologously (from the patient's own blood) or allogeneically (from a certified donor), based on the patient's immune profile and clinical assessment. Preparation and quality testing performed in our Warsaw laboratory.

Biological Mechanisms

  • Suppress residual cytokine storm mediators that sustain alveolar inflammation
  • Restore immune homeostasis in the pulmonary microenvironment
  • Reduce immune-mediated endothelial injury in the pulmonary vasculature

How This Helps in Post-COVID Lung Damage

Many post-COVID patients have a measurably dysregulated immune profile months after infection — elevated inflammatory markers, persistent T-cell activation and impaired regulatory immune function. T-regs directly address this by restoring the balance between pro-inflammatory and regulatory immune responses, reducing ongoing tissue damage and allowing the lung's repair mechanisms to function.

Your Medical Board

The exact combination, dosage, sequencing and delivery method of all five components is determined individually by our medical board for each patient. No two treatment protocols are identical. Your programme is constructed based on your specific diagnosis, imaging findings, pulmonary function data, inflammatory markers and clinical priorities.

Your protocol is designed individually. Speak with our medical team to understand what your personalised program would include.

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Patient Journey

Your Treatment Journey
Step by Step

01

Free Medical Consultation

Your case is reviewed remotely by our physician team. We assess your diagnosis, current pulmonary function, imaging findings, medical history and treatment goals. This consultation is free and carries no obligation.

02

Medical Eligibility Assessment

A detailed review of all medical documentation — including HRCT scans, spirometry, DLCO measurements and relevant blood work. Our medical board evaluates eligibility, confirms safety parameters and designs your personalised therapeutic protocol.

03

Laboratory Preparation

Your cells are collected, isolated, expanded and quality-tested in our certified Warsaw laboratory. Each batch receives a full traceability certificate. This stage typically takes 2–3 weeks.

04

Treatment Administration

Cells are delivered by intravenous infusion — no surgery, no general anaesthesia. Airport transfers, accommodation and visa support are included in the programme for international patients.

05

Supervised Respiratory Rehabilitation

Structured pulmonary rehabilitation sessions with our specialist, adapted to your current respiratory capacity and exercise tolerance. Available at our clinic or remotely coordinated with your local physiotherapy team.

06

Long-Term Medical Follow-Up

Your dedicated coordinator monitors respiratory function, tracks spirometry and imaging changes, and adjusts recommendations based on your recovery data. A medical-grade wearable bracelet supports continuous oxygen saturation and activity tracking regardless of your location.

01

Free Medical Consultation

Your case is reviewed remotely by our physician team. We assess your diagnosis, current pulmonary function, imaging findings, medical history and treatment goals. This consultation is free and carries no obligation.

02

Medical Eligibility Assessment

A detailed review of all medical documentation — including HRCT scans, spirometry, DLCO measurements and relevant blood work. Our medical board evaluates eligibility, confirms safety parameters and designs your personalised therapeutic protocol.

03

Laboratory Preparation

Your cells are collected, isolated, expanded and quality-tested in our certified Warsaw laboratory. Each batch receives a full traceability certificate. This stage typically takes 2–3 weeks.

04

Treatment Administration

Cells are delivered by intravenous infusion — no surgery, no general anaesthesia. Airport transfers, accommodation and visa support are included in the programme for international patients.

05

Supervised Respiratory Rehabilitation

Structured pulmonary rehabilitation sessions with our specialist, adapted to your current respiratory capacity and exercise tolerance. Available at our clinic or remotely coordinated with your local physiotherapy team.

06

Long-Term Medical Follow-Up

Your dedicated coordinator monitors respiratory function, tracks spirometry and imaging changes, and adjusts recommendations based on your recovery data. A medical-grade wearable bracelet supports continuous oxygen saturation and activity tracking regardless of your location.

The first step is free. Request a medical consultation and our medical consultant will contact you within 24 hours.

Request Consultation

Safety Profile

Safety, Eligibility
and Contraindications

Cellular therapy is considered safe when delivered under proper medical supervision and according to validated protocols. In our practice, the procedure is well-tolerated by the majority of patients with post-COVID lung damage.

Temporary mild reactions — such as transient low-grade fever, slight fatigue or mild discomfort at the infusion site — may occur in a minority of patients. These are typically short-lived and indicate active immune engagement.

A final medical assessment is performed on-site before every treatment session. If a patient's respiratory status has deteriorated — including acute exacerbation or new infection — the programme may be temporarily modified or postponed for safety reasons.

All contraindications are evaluated individually. A contraindication in one clinical context does not necessarily preclude treatment in a different context — this is always determined by physician assessment.

Standard Contraindications

Active acute infection or fever

Active malignancy or ongoing chemotherapy / radiotherapy

Severe decompensated cardiac or renal failure

Pregnancy

Active pulmonary embolism or untreated deep vein thrombosis

Post-Treatment

After Treatment
and Follow-Up

01

Dedicated respiratory rehabilitation specialist

monitors lung function, exercise tolerance and oxygen saturation trends

02

Personalised pulmonary rehabilitation programme

graded breathing exercises, aerobic conditioning, respiratory muscle training

03

Medical-grade wearable monitoring

continuous SpO₂ and activity data supporting clinical decision-making

04

Long-term coordinator support

proactive check-ins, clinical guidance and response to any changes in respiratory status

05

Follow-up imaging and spirometry

scheduled HRCT and pulmonary function testing to objectively track structural and functional recovery

Pulmonary tissue repair is a gradual biological process. Measurable improvement on spirometry and imaging typically lags behind subjective symptom improvement by several weeks. Consistent follow-up and adherence to the rehabilitation protocol are essential for sustained results.

Patient Stories

What Our Patients Say

01 / 05

“Six months after COVID I was still on oxygen at home. My doctors in Lyon said the scarring had stabilised but would not get better. Within a few months of the programme, I could walk to work again without stopping. I breathe easier, sleep better, and my last scan showed real clearing.”

Patient

Post-COVID Pulmonary Fibrosis · France

Every case is assessed individually by our physician team. Request a consultation to discuss your specific situation with our physician team.

Request Consultation

Patient Cases

Clinical Observations

Documented treatment outcomes recorded by the BioCells Medical team after personalised regenerative medicine protocols.

All cases →
ALS — Regained Movements and Improved Swallowing
Neurological·July 2025

ALS — Regained Movements and Improved Swallowing

Amyotrophic Lateral Sclerosis

Ilaria Baldi · Italy→
Parkinsonism — Reduced Rigidity, Improved Walking and Clearer Speech
Neurological·March 2025

Parkinsonism — Reduced Rigidity, Improved Walking and Clearer Speech

Parkinsonism

Franco Bonifazi · Italy→
COPD — Improved Breathing Capacity and Physical Endurance
Respiratory·September 2024

COPD — Improved Breathing Capacity and Physical Endurance

Chronic Obstructive Pulmonary Disease

Pier Giorgio · Italy→
Multiple Sclerosis — Regained Strength and Restored Independence
Neurological·May 2024

Multiple Sclerosis — Regained Strength and Restored Independence

Secondary Progressive Multiple Sclerosis (SPMS)

Silvia Baistrocchi · Italy→

Get Started

Take the First Step

If you are living with persistent respiratory complications after COVID-19, our medical team is available for a free, no-obligation medical consultation — based on your diagnosis, imaging findings and current pulmonary function.

We review every inquiry personally. You will speak with a physician, not an administrator.

01

Submit your case online or by phone

02

Our medical consultant contacts you to review your documents

03

The medical board presents your personalised treatment plan

Request a Consultation

Tell us about your condition. Our medical consultant will contact you within 24 hours to review your documents.

Open Consultation Form
info@biocellsmedical.com
+48 22 307 48 82EN / RU / PL+44 20 8073 1427UK+39 392 995 41 31IT+33 4 23 11 00 21FR

Multilingual coordination — English, Italian, French, Russian, Polish

Evidence Base

Scientific References
and Clinical Trials

Our clinical approach is informed by and consistent with published research in the field of regenerative medicine.

Mesenchymal Stem Cell Therapy for COVID-19-Induced ARDS — Randomized Clinical Trial

pubmed.ncbi.nlm.nih.gov/34380007/

↗

Umbilical Cord MSC Treatment for Long COVID Pulmonary Sequelae — Phase 1 Trial

pubmed.ncbi.nlm.nih.gov/36723563/

↗

Efficacy and Safety of MSC Therapy in COVID-19 Patients — Systematic Review and Meta-Analysis

pubmed.ncbi.nlm.nih.gov/35979368/

↗

Post-COVID Pulmonary Fibrosis: Therapeutic Potential of Mesenchymal Stem Cells

pubmed.ncbi.nlm.nih.gov/37120782/

↗

Exosome-Based Therapies for Lung Injury and Fibrosis — Current Evidence and Future Directions

pubmed.ncbi.nlm.nih.gov/36325525/

↗