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BioCells MedicalBioCells Medical

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

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BIRTH ASPHYXIA · NEONATAL ENCEPHALOPATHY · HYPOXIC-ISCHEMIC ENCEPHALOPATHY

Hypoxic-Ischemic Brain Injury (HIE): Personalised Cellular Therapy

A physician-led, laboratory-verified treatment programme targeting the neurological consequences of oxygen deprivation — designed to support motor development, cognitive recovery and neuroplasticity based on the individual injury pattern, age and clinical profile of each patient.

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About the Condition

What is Hypoxic-Ischemic Brain Injury?

Hypoxic-ischemic brain injury (HIE) occurs when the brain is deprived of adequate oxygen and blood flow. The resulting cellular damage triggers a cascade of neuronal death, white matter injury and chronic neuroinflammation that can persist long after the initial insult.

In neonates, HIE is most commonly caused by birth asphyxia — complications during labour and delivery that interrupt placental blood flow. In older children and adults, cardiac arrest, near-drowning, severe hypotension or perioperative complications can produce the same pattern of injury.

HIE is an acute injury with chronic consequences. The severity depends on the duration and degree of oxygen deprivation, the brain regions affected, and the age at which the injury occurred. Earlier intervention generally produces better clinical outcomes — the developing brain retains significant neuroplastic potential that diminishes over time.

01

Neonatal HIE (Birth Asphyxia)

The most common form, resulting from oxygen deprivation during labour, delivery or the immediate postnatal period. Affects 1–3 per 1,000 live births in developed countries. Severity is graded using the Sarnat classification (mild, moderate, severe). Motor, cognitive and developmental consequences depend on the extent and location of brain injury.

02

Cardiac Arrest HIE

Occurs in children or adults following cardiac arrest with prolonged cerebral hypoperfusion. The duration of circulatory arrest is the primary determinant of injury severity. Global cerebral ischaemia typically affects the hippocampus, basal ganglia and cortical watershed zones. Recovery potential depends on the interval between arrest and restoration of circulation.

03

Near-Drowning HIE

Results from submersion injury with prolonged hypoxia. Predominantly affects paediatric patients. The injury pattern is similar to cardiac arrest HIE but often involves additional hypothermia-related factors. Younger patients may retain greater neuroplastic recovery potential.

04

Perioperative HIE

Occurs as a complication of surgical procedures — typically cardiac surgery, major vascular surgery or procedures requiring prolonged anaesthesia. The injury mechanism involves transient cerebral hypoperfusion during or immediately after the procedure. Severity varies from focal deficits to diffuse cortical injury.

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 the nature and timing of the hypoxic-ischemic event, current neurological status, imaging findings and developmental trajectory.

The BioCells Program

How We Treat
Five-Component Protocol

Our HIE 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 injury pattern, developmental status, age 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 paediatric HIE patients, where repeated anaesthesia exposure carries additional neurodevelopmental risks.

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 biological mechanisms limiting recovery

Our protocol addresses chronic neuroinflammation, impaired myelination, excitotoxicity and oxidative stress — the persistent biological barriers to neurological recovery after hypoxic-ischemic injury.

Complements existing rehabilitation

Our programme works alongside ongoing physiotherapy, occupational therapy and developmental interventions. Patients do not need to discontinue any existing rehabilitation or medication.

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 responsible for suppressing excessive inflammatory responses in the nervous system. After hypoxic-ischemic injury, the immune system often shifts into a chronically activated state that causes ongoing secondary damage to brain tissue.

How It Is Done

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

Biological Mechanisms

  • Suppress the secondary inflammatory cascade that extends brain damage after the initial injury
  • Reduce immune-mediated destruction of surviving neurons and glial cells
  • Restore neuro-immune homeostasis in the injured brain

How This Helps in Hypoxic-Ischemic Brain Injury

The secondary injury phase in HIE is driven largely by excessive immune activation — microglia and infiltrating immune cells produce pro-inflammatory cytokines that damage tissue the initial hypoxic event left intact. T-regs directly counteract this process, limiting secondary damage and preserving the neural substrate needed for functional recovery.

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 injury pattern, neurological status, age, 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 the nature and timing of the hypoxic-ischemic event, current neurological status, imaging findings and developmental trajectory. This consultation is free and carries no obligation.

02

Medical Eligibility Assessment

A detailed review of all medical documentation — including MRI findings, developmental assessments and rehabilitation records. Our medical board evaluates eligibility, confirms safety parameters and designs your personalised therapeutic protocol.

03

Laboratory Preparation

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 rehabilitation sessions with our specialist, adapted to the patient's age, injury pattern and current functional level. Paediatric protocols incorporate developmental milestones and age-appropriate therapeutic approaches. Available at our clinic or remotely coordinated with your local medical team.

06

Long-Term Medical Follow-Up

Your dedicated coordinator monitors neurological status, developmental progress and overall well-being. A medical-grade wearable bracelet supports continuous health tracking regardless of your location. Follow-up assessments are scheduled at regular intervals to document progress and guide ongoing care.

01

Free Medical Consultation

Your case is reviewed remotely by our physician team. We assess the nature and timing of the hypoxic-ischemic event, current neurological status, imaging findings and developmental trajectory. This consultation is free and carries no obligation.

02

Medical Eligibility Assessment

A detailed review of all medical documentation — including MRI findings, developmental assessments and rehabilitation records. Our medical board evaluates eligibility, confirms safety parameters and designs your personalised therapeutic protocol.

03

Laboratory Preparation

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 rehabilitation sessions with our specialist, adapted to the patient's age, injury pattern and current functional level. Paediatric protocols incorporate developmental milestones and age-appropriate therapeutic approaches. Available at our clinic or remotely coordinated with your local medical team.

06

Long-Term Medical Follow-Up

Your dedicated coordinator monitors neurological status, developmental progress and overall well-being. A medical-grade wearable bracelet supports continuous health tracking regardless of your location. Follow-up assessments are scheduled at regular intervals to document progress and guide ongoing care.

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 both paediatric and adult HIE patients.

Temporary mild reactions — such as transient low-grade temperature, slight irritability in young children or mild fatigue — may occur in a minority of patients. These are typically short-lived and indicate active biological engagement.

A final medical assessment is performed on-site before every treatment session. If a patient's status has changed — including seizure activity or acute illness — 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

Uncontrolled epileptic status (active seizure disorder must be stabilised prior to treatment)

Post-Treatment

After Treatment
and Follow-Up

01

Dedicated rehabilitation specialist

monitors motor development, cognitive milestones and overall neurological status

02

Personalised rehabilitation programme

adapted to the patient's age, injury pattern and current developmental stage

03

Medical-grade wearable monitoring

continuous physiological data collection supporting clinical decision-making

04

Long-term coordinator support

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

05

Continued clinical access

our medical team remains available for ongoing reassessment and protocol adjustment

Neurological recovery after hypoxic-ischemic injury follows a non-linear trajectory. Biological repair processes — remyelination, synaptic reorganisation, resolution of chronic inflammation — require sustained clinical oversight. The post-treatment period is integral to the therapeutic programme.

Patient Stories

What Our Patients Say

01 / 05

“Amir was eighteen months old and could not hold his head up. After the programme he started lifting it on his own during tummy time. His physiotherapist confirmed the change. Tone in his neck and trunk had improved. The gap between him and other children his age is closing rather than widening, and that distinction matters enormously to us.”

Patient's mother

Neonatal HIE (birth asphyxia) · UAE

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

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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 your child or someone you love has been diagnosed with hypoxic-ischemic brain injury, our medical team is available for a free, no-obligation medical consultation — based on the diagnosis, current neurological status 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.

Feasibility of Autologous Cord Blood Cells for Infants with Hypoxic-Ischemic Encephalopathy (Cotten et al., J Pediatr, 2014)

pubmed.ncbi.nlm.nih.gov/24388332/

↗

Autologous Cord Blood Cell Therapy for Neonatal Hypoxic-Ischaemic Encephalopathy: A Pilot Study for Feasibility and Safety (Sci Rep, 2020)

pubmed.ncbi.nlm.nih.gov/32165664/

↗

Stem Cell-Based Interventions for the Prevention of Morbidity and Mortality Following Hypoxic-Ischaemic Encephalopathy in Newborn Infants (Cochrane Database Syst Rev, 2020)

pubmed.ncbi.nlm.nih.gov/32813884/

↗

Stem Cell Therapy for Neonatal Hypoxic-Ischemic Encephalopathy: A Systematic Review of Preclinical Studies (Int J Mol Sci, 2021)

pubmed.ncbi.nlm.nih.gov/33808671/

↗

Translational Potential of Stem Cell-based Therapies in the Treatment of Neonatal Hypoxic-Ischemic Brain Injury (Stem Cell Rev Rep, 2025)

pubmed.ncbi.nlm.nih.gov/40471437/

↗

Monitoring of Outcomes of Cellular and Exosome-based Therapies in Autoinflammatory and Post-infectious Neuroinflammatory Syndromes — ClinicalTrials.gov (NCT07145502)

clinicaltrials.gov/study/NCT07145502

↗