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BioCells MedicalBioCells Medical

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

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CHRONIC BRONCHITIS · EMPHYSEMA · COPD GOLD STAGES II–IV

COPD: Personalised Cellular Therapy

A physician-led, laboratory-verified treatment programme targeting the biological mechanisms behind airflow limitation, alveolar destruction and chronic airway inflammation — tailored to the individual phenotype, GOLD stage and clinical profile of each COPD patient.

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About the Condition

What is COPD?

Chronic Obstructive Pulmonary Disease (COPD) is a progressive respiratory condition characterised by persistent airflow limitation, chronic inflammation of the airways and destruction of alveolar tissue. The two principal pathological components — emphysema (destruction of air sacs) and chronic bronchitis (chronic mucus-producing inflammation of the bronchi) — frequently coexist in varying proportions.

As the disease advances, gas exchange deteriorates, exercise tolerance declines and exacerbations become more frequent. The resulting cycle of inflammation, tissue remodelling and loss of elastic recoil leads to progressive respiratory insufficiency that standard bronchodilator and corticosteroid therapy can manage symptomatically but cannot reverse.

COPD affects over 380 million people globally and remains the third leading cause of death worldwide. Current pharmacological management stabilises symptoms but does not address the underlying alveolar destruction or chronic inflammatory pathology — which is the focus of our cellular therapy programme.

01

Emphysema-predominant

Characterised primarily by destruction of the alveolar walls, leading to enlarged air spaces, reduced gas exchange surface area and loss of lung elastic recoil. Patients typically present with progressive breathlessness, hyperinflation and reduced diffusion capacity. Often associated with lower BMI and significant exercise limitation.

02

Chronic Bronchitis-predominant

Defined by chronic productive cough for at least three months in two consecutive years. Airway inflammation, goblet cell hyperplasia and excess mucus production are the dominant features. Patients are more prone to infectious exacerbations and airway obstruction from mucus plugging.

03

COPD-Asthma Overlap (ACO)

Patients exhibit features of both COPD and asthma — persistent airflow limitation combined with eosinophilic inflammation and partial bronchodilator reversibility. Represents approximately 15–20% of COPD diagnoses. Typically associated with earlier onset, more frequent exacerbations and distinct inflammatory profiles requiring adapted therapeutic strategy.

04

Frequent Exacerbator Phenotype

Defined by two or more moderate exacerbations or one hospitalisation per year. Exacerbations accelerate lung function decline, increase mortality risk and significantly impair quality of life. This phenotype persists independently of GOLD stage and requires targeted anti-inflammatory intervention beyond standard inhaler therapy.

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 diagnosis, GOLD stage, exacerbation history, pulmonary function tests and overall clinical profile.

The BioCells Program

How We Treat
Five-Component Protocol

Our COPD 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, disease phenotype, inflammatory markers and clinical priorities.

Minimally invasive administration

Treatment is delivered by intravenous infusion or targeted local injection using specialised medical systems — not surgical instruments.

No general anaesthesia

Particularly important in COPD, where compromised respiratory function may make general anaesthesia high-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 airflow limitation with bronchodilators alone, our protocol targets alveolar destruction, chronic inflammation and immune dysregulation — the biological drivers of COPD progression.

Complements existing medication

Our programme is compatible with all standard COPD medications including inhaled corticosteroids, long-acting bronchodilators and phosphodiesterase inhibitors. Patients do not need to discontinue existing treatment.

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 excessive and self-destructive inflammatory responses. In healthy lungs, they maintain immune homeostasis; in COPD, their function is impaired, contributing to the cycle of chronic inflammation and progressive tissue destruction.

How It Is Done

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

Biological Mechanisms

  • Restore immune regulation within chronically inflamed airways
  • Suppress the excessive neutrophilic and CD8+ T-cell response driving airway remodelling
  • Reduce the systemic inflammatory burden associated with COPD exacerbations and comorbidities

How This Helps in COPD

COPD is fundamentally an immune-mediated disease — persistent activation of innate and adaptive immune pathways sustains chronic airway inflammation even years after smoking cessation. T-regs counteract this by restoring the balance between pro-inflammatory and anti-inflammatory signalling, reducing neutrophilic tissue damage and stabilising the immune environment to lower exacerbation risk.

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, COPD phenotype, GOLD stage, biological 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 GOLD stage, pulmonary function data, exacerbation history and treatment goals. This consultation is free and carries no obligation.

02

Medical Eligibility Assessment

A detailed review of all medical documentation including spirometry, CT imaging and 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 laboratory. Each batch receives a full traceability certificate. This stage typically takes 2–3 weeks.

04

Treatment Administration

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

05

Supervised Rehabilitation

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

06

Long-Term Medical Follow-Up

Your dedicated coordinator monitors respiratory status, exacerbation frequency, spirometry trends and overall well-being. A medical-grade wearable bracelet supports continuous health tracking regardless of your location.

01

Free Medical Consultation

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

02

Medical Eligibility Assessment

A detailed review of all medical documentation including spirometry, CT imaging and 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 laboratory. Each batch receives a full traceability certificate. This stage typically takes 2–3 weeks.

04

Treatment Administration

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

05

Supervised Rehabilitation

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

06

Long-Term Medical Follow-Up

Your dedicated coordinator monitors respiratory status, exacerbation frequency, spirometry trends and overall well-being. A medical-grade wearable bracelet supports continuous health 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 COPD patients.

Temporary mild reactions — such as transient local discomfort at the infusion site, slight fatigue or low-grade temperature — 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 changed — including acute exacerbation or active 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 respiratory infection or pneumonia

Active malignancy or ongoing chemotherapy / radiotherapy

Acute COPD exacerbation requiring hospitalisation (treatment postponed until stable)

Severe decompensated cardiac or renal failure

Pregnancy

Post-Treatment

After Treatment
and Follow-Up

01

Dedicated pulmonary rehabilitation specialist

monitors respiratory function, exercise capacity and exacerbation patterns

02

Personalised home rehabilitation programme

breathing exercises, respiratory muscle training and graded activity protocols adapted to your current capacity

03

Medical-grade wearable monitoring

continuous oxygen saturation, heart rate 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

Continued clinical access

our medical team remains available for ongoing reassessment, spirometry review and protocol adjustment

Pulmonary tissue repair follows a gradual biological timeline. The weeks and months following treatment are clinically critical — consistent rehabilitation, monitoring and medical follow-up directly influence long-term respiratory outcomes.

Patient Stories

What Our Patients Say

01 / 05

“I was on supplemental oxygen at home and could barely walk to the kitchen. After treatment I started getting through the mornings without reaching for the cannula. I can walk the dog again. For eight years everything went in one direction. Now it has shifted.”

Patient

COPD (emphysema-predominant, GOLD III) · United Kingdom

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 or someone you care about has been diagnosed with COPD, our medical team is available for a free, no-obligation medical consultation — based on your diagnosis, current GOLD stage and individual clinical profile.

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

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 Stromal Cell Therapy for Chronic Obstructive Pulmonary Disease: A Systematic Review and Meta-Analysis (Sun et al., 2020)

pubmed.ncbi.nlm.nih.gov/32709836/

↗

A Randomized, Double-Blind, Placebo-Controlled Trial of Allogeneic Human Mesenchymal Stem Cells in Patients with Moderate COPD (Weiss et al., 2013)

pubmed.ncbi.nlm.nih.gov/23992272/

↗

Safety and Feasibility of Autologous Bone Marrow-Derived Mesenchymal Stem Cells in COPD (Stolk et al., 2016)

pubmed.ncbi.nlm.nih.gov/26851002/

↗

Extracellular Vesicles in Chronic Obstructive Pulmonary Disease: Pathogenesis and Therapeutic Potential (Kadota et al., 2022)

pubmed.ncbi.nlm.nih.gov/35071107/

↗

Mesenchymal Stem Cell-Derived Exosomes Attenuate Cigarette Smoke-Induced Lung Inflammation and Injury (Kim et al., 2022)

pubmed.ncbi.nlm.nih.gov/34856523/

↗