Age-related macular degeneration (AMD) affects 2 million people in France and is the main cause of irreversible blindness in France. All patients initially have an early form of the disease. This early form can evolve in two different ways: the atrophic form, which progresses slowly, and the exudative or neovascular form, which has a more rapid evolution. While there are treatments for the exudative form of the disease, there is currently no therapy for the atrophic form of AMD. Recently, it has been demonstrated in atrophic AMD that there is accumulation of inflammatory cells, monocytes, in the sub-retinal space. This space is located between the retinal pigment epithelium (RPE) and photoreceptors. It is physiologically devoid of immune cells (immune privilege). Monocytes secrete many pro-inflammatory molecules, such as cytokines. Some cytokines (IL-1, IL6 and TNF) have a deleterious role on RPE and photoreceptors in mouse models. The identification of specific cytokines would help to better understand this disease and consider potential targeted therapies. Our project is based on the hypothesis that monocytes extracted from patients with AMD have a superior survival on RPE compared to monocytes extracted from healthy patients (without retinal pathology), and more particularly in atrophic forms of AMD. The main aim of this study is to compare the survival of monocytes extracted from patients with atrophic AMD to monocytes extracted from patients without retinal pathology (control) on retinal pigment epithelial cell lines (ARPE-19). Survival will be evaluated by automated counting of monocytes after 24 hours of culture on ARPE-19 after specific immunostaining of monocytes. If the survival of monocytes from patients with the late form of AMD is increased then therapy directly targeting this pathological accumulation of monocytes could be considered. Moreover, the identification of increased secretion of certain cytokines and the demonstration of their deleterious effect on retinal physiology could lead to targeted therapies against them.
Male or female older than 50,
Provide written informed consent,
Patient affiliated to French social security,
Maximum sampling volume (care + research) per 30-day period to be adapted according to the weight of the patient
Patient whose weight is less than 50kg,
Adult patient under guardianship or curatorship or unable to express consent,
Person deprived of liberty,
Patient participating in an ongoing clinical trial during the inclusion visit,
Parallel
Blood samples
Other intervention: The blood sample from all groups will be taken on the day of inclusion, in the ophthalmology department. The patient will be cared for by a nurse and then taken to the collection room. A 100 ml sample will be taken (10 tubes of 10 ml). Blood samples will be labeled with the patient's identification number as part of the protocol. They will be transported to the research laboratory in order to be picked up for monocyte extraction. The purification of blood monocytes will be done. In case of excess, the samples will be destroyed at the end of the study.
Comparison of the survival of human monocytes on ARPE-19 cultures, between the group of patients with atrophic AMD and patient with no retinal pathology (control).
Survival will be evaluated by automated counting of monocytes
Comparison of human monocyte survival on ARPE-19 cell lines between different groups of patients with AMD or according to severity of disease.
Survival will be assessed by automated counting of monocytes on the culture plate after specific immunostaining of the monocytes.
Comparison of alterations in ARPE-19 cells lines after culture by human monocytes:
Comparison of alterations in ARPE-19 cells lines after culture by human monocytes: * Between the atrophic AMD group and the control group, * With respect to the stage of the AMD (early / intermediate AMD, exudative or atrophic AMD), * With respect to the evolving profile of atrophic AMD defined by autofluorescence examination, * With respect to the severity of the clinical involvement of atrophic AMD, * With respect to the recognized risk factors of the disease (age, sex, smoking status and obesity). The alteration of ARPE-19 cells on expression level of OTX2, a ubiquitous transcription factor in EPR cells, will be studied. OTX2 is normally under-expressed in-vitro when a supernatant of lipopolysaccharide-activated monocytes is added to the culture medium.
To compare the secretion of IL1 from patient's monocytes:
To compare the secretion of IL1 from patient's monocytes: * Between the atrophic AMD group and the control group, With respect to the stage of the AMD (early / intermediate AMD, exudative or atrophic AMD), * With respect to the evolving profile of atrophic AMD defined by autofluorescence examination, * With respect to the severity of the clinical involvement of atrophic AMD, * With respect to the recognized risk factors of the disease (age, sex, smoking status and obesity). The secretory activity of monocytes on the following cytokines will be evaluated : IL1, IL6 and TNF by two techniques: qPCR and ELISA.
To compare the secretion of IL6 from patient's monocytes:
To compare the secretion of IL6 from patient's monocytes:
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