Stem Cells,
Information and prospects.

The stem cells of the umbilical cord, cord tissue, and placenta

When a baby is born, a unique biological resource is born with it: the umbilical cord and the placenta. For decades, they were considered mere “waste” of childbirth; today we know that, on the contrary, they hold one of the most precious treasures of modern medicine: stem cells.

These cells are not all the same: in the cord blood, in the tissue that surrounds it, and in the placenta, there are different populations, each with particular characteristics. Together, they form an extraordinary biological arsenal, capable of helping in the treatment of diseases that are already treatable today and opening up prospects for future therapies.

Cord blood: hematopoietic cells

The blood of the umbilical cord concentrates hematopoietic stem cells, which give rise to all blood cells: red blood cells, white blood cells, and platelets.

They are the most “famous” cells because they have already changed the lives of thousands of patients: they are used in transplants for more than 80 diseases, particularly blood disorders such as leukemias, lymphomas, thalassemias, and severe immunodeficiencies.

  • Acute lymphoblastic leukemia
  • Acute myeloid leukemia
  • Biphenotypic acute leukemia
  • Undifferentiated acute leukemia
  • Adult T-cell leukemia/lymphoma
  • Hodgkin lymphoma
  • Non-Hodgkin lymphomas
  • Chronic lymphocytic leukemia
  • Prolymphocytic leukemia
  • Myelodysplastic syndromes, including:
    • Refractory anemia
    • Refractory anemia with ringed sideroblasts
    • Refractory anemia with excess blasts
    • Refractory anemia with excess blasts in transformation
  • Chronic myelomonocytic leukemia
  • Juvenile myelomonocytic leukemia
  • Refractory cytopenia
  • Philadelphia positive chronic myeloid leukemia
  • Idiopathic myelofibrosis
  • Polycythemia vera
  • Essential thrombocythemia
  • Multiple myeloma
  • Plasma cell leukemia
  • Waldenström macroglobulinemia
  • Amyloidosis
  • Acquired aplastic anemia
  • Fanconi anemia
  • Congenital dyskeratosis
  • Paroxysmal nocturnal hemoglobinuria
  • Blackfan-Diamond anemia
  • Congenital dyserythropoietic anemia
  • Acquired pure red cell aplasia
  • Congenital amegakaryocytic thrombocytopenia (due to mutation of the thrombopoietin receptor gene)
  • Congenital platelet disorders (e.g. Bernard-Soulier disease, Glanzmann’s thrombasthenia)
  • Congenital agranulocytosis (Kostmann syndrome)
  • Shwachman-Diamond syndrome
  • Beta thalassemia
  • Sickle cell anemia
  • Selected cases of pyruvate kinase deficiency with transfusion dependence
  • Familial hemophagocytic lymphohistiocytosis
  • Griscelli syndrome
  • Chediak-Higashi syndrome
  • Langerhans cell histiocytosis (Histiocytosis X)
  • Chronic granulomatous disease
  • Deficiency of leukocyte adhesion proteins
  • Severe combined immunodeficiencies (SCID), including:
    • Adenosine deaminase deficiency
    • Defect of class I and II HLA molecules
    • Zap70 deficiency
    • Omenn syndrome
    • Purin-nucleoside-phosphorylase deficiency
    • Reticular dysgenesis
    • Defect of the common γ chain for multiple cytokines
    • JAK3 deficiency
    • Hyper-IgM syndrome
    • Wiskott-Aldrich syndrome
    • X-linked lymphoproliferative syndrome (Duncan/Purtillo syndrome)
  • Cartilage-capitellum hypoplasia
  • DiGeorge syndrome
  • IPEX syndrome (immunodeficiency with polyendocrinopathy, enteropathy, X-linked)
  • Hurler Syndrome (MPS-IH)
  • Scheie Syndrome (MPS-IS)
  • Maroteaux-Lamy Syndrome (MPS-VI)
  • Sly Syndrome (MPS-VII)
  • Adrenoleukodystrophy
  • Fucosidosis
  • Gaucher Disease
  • Krabbe Disease
  • Manosidosis
  • Metachromatic leukodystrophy
  • Mucolipidosis II (I-cell disease)
  • Neuronal ceroid lipofuscinosis (Batten disease)
  • Sandhoff Disease
  • Osteopetrosis
  • Osteogenesis imperfecta
  • Other hereditary disorders
  • Congenital erythropoietic porphyria (Gunther)
  • Ewing’s Sarcoma
  • Neuroblastoma
  • Clear Cell Carcinoma of the Kidney
  • Rhabdomyosarcoma
  • Other Neoplasms
  • Evans Syndrome
  • Autoimmune Lymphoproliferative Syndromes (due to FAS, FAS-L, caspase deficiency)
  • Progressive Systemic Sclerosis
  • Pediatric Neoplasms Treated with Chemotherapy / Radiotherapy

The immunological advantage: compared to bone marrow, cord blood is more “tolerant.” This means that even if the compatibility between donor and recipient is not perfect, the risk of rejection is lower. It’s as if cord cells are younger and less “rigid” in recognizing what is foreign, which makes them valuable in transplants.

Cord tissue: mesenchymal cells

The tissue that surrounds the cord vessels, called Wharton’s jelly, is rich in mesenchymal stromal cells (MSC). These cells have another type of power: they can transform into bones, cartilage, muscles, and adipose tissue.

Differentiative characteristics: MSCs are not used to reconstruct blood, but to regenerate solid tissues and modulate inflammation. They are “architect” cells, capable of contributing to the repair of damaged tissues.

The immunological advantage: MSCs have a natural ability to calm the immune system. For this reason, they are being studied for autoimmune diseases (such as multiple sclerosis or lupus), to regenerate the heart after a heart attack, or to repair cartilage and bones.

Placenta: a double treasure

The placenta is often overlooked, yet it is a true treasure trove of stem cells. It contains both hematopoietic cells, similar to those in cord blood, and mesenchymal cells, like those in cord tissue. In other words, a double biological heritage.

In addition to its clinical potential, the placenta has another unique characteristic: it is naturally programmed to manage the immune dialogue between mother and fetus. Placental cells inherit this ability, becoming interesting tools for future therapies that require immune tolerance and inflammation control.

Why keep them?

Why it is a unique opportunity: blood, tissue, and placenta can only be collected at birth, using simple, non-invasive, and completely safe procedures.

Why they are already useful today: cord blood has been used for over twenty years in life-saving transplants for blood and immune system diseases.

Why they offer prospects for tomorrow: mesenchymal and placental cells are being studied for innovative applications in neurology, cardiology, orthopedics, oncology, and autoimmune diseases.

Storing these cells means safeguarding a biological asset that belongs to the child and, in some cases, may also be useful for compatible siblings or parents.

In summary: the cord and placenta are not just “memories of birth,” but therapeutic and regenerative resources that one day could make the difference between having or not having a treatment available.

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